Mechanism of Crosstalk between m6A Modification and Epigenetic Regulation
Crosstalk ID
M6ACROT05686
[1]
m6A modification Circ_MYO1C Circ_MYO1C METTL3 Methylation : m6A sites Direct Enhancement Non-coding RNA circMYO1C CD274  lncRNA       miRNA   circRNA
m6A Modification:
m6A Regulator Methyltransferase-like 3 (METTL3) WRITER
m6A Target Circ_MYO1C
Epigenetic Regulation that have Cross-talk with This m6A Modification:
Epigenetic Regulation Type Non-coding RNA (ncRNA)
Epigenetic Regulator Circ_MYO1C circRNA View Details
Regulated Target CD274 molecule (CD274) View Details
Crosstalk Relationship m6A  →  ncRNA Enhancement
Crosstalk Mechanism m6A regulators directly modulate the functionality of ncRNAs through specific targeting ncRNA
Crosstalk Summary Mechanistically, Circ_MYO1C cyclization was mediated by m6A methyltransferase METTL3. Moreover, methylated RNA immunoprecipitation sequencing (MeRIP-seq) unveiled the remarkable m6A modification on CD274 molecule (CD274) mRNA. Moreover, circMYO1C targeted the m6A site of PD-L1 mRNA to enhance its stability by cooperating with IGF2BP2, thereby accelerating PDAC immune escape.
Responsed Disease Pancreatic ductal adenocarcinoma ICD-11: 2C10.0
Cell Process Cell proliferation
Cell migration
In-vitro Model
PANC-1 Pancreatic ductal adenocarcinoma Homo sapiens CVCL_0480
Capan-2 Pancreatic ductal adenocarcinoma Homo sapiens CVCL_0026
BxPC-3 Pancreatic ductal adenocarcinoma Homo sapiens CVCL_0186
CFPAC-1 Cystic fibrosis Homo sapiens CVCL_1119
In-vivo Model Male BALB/c nude mice (5-6 weeks) were obtained from Slac Laboratory Animal Center (Shanghai, China) and maintained under pathogen-free conditions. PANC-1 cells (2 × 106 cells suspended in 100 μl PBS) transfected with circMYO1C knockdown (sh-circMYO1C) or controls (sh-NC) were subcutaneously injected into the flank of nude mice. One week later, the tumor size was measured every three days.
Full List of Potential Compound(s) Related to This m6A-centered Crosstalk
CD274 molecule (CD274) 55 Compound(s) Regulating the Target Click to Show/Hide the Full List
 Compound Name Avelumab Approved [2]
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 Compound Name Durvalumab Approved [3]
MOA Modulator
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 Compound Name RG-7446 Approved [4]
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 Compound Name Bavencio Approved [5]
MOA Inhibitor
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 Compound Name Atezolizumab Approved [6]
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 Compound Name Sugemalimab Approved in China [7]
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 Compound Name MEDI4736 Phase 3 [8]
MOA Modulator
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 Compound Name MPDL-3280A Phase 3 [9]
MOA Modulator
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 Compound Name CS1001 Phase 3 [10]
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 Compound Name A167 Phase 3 [11]
Synonyms
KL-A167
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 Compound Name KN046 Phase 3 [12]
MOA Inhibitor
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 Compound Name Pidilizumab Phase 2 [13]
Synonyms
CT-011
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 Compound Name KN035 Phase 2 [14]
Synonyms
Envafolimab
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 Compound Name CX-072 Phase 2 [15]
MOA Inhibitor
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 Compound Name INCB86550 Phase 2 [16]
MOA Inhibitor
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 Compound Name Bintrafusp alfa Phase 2 [17]
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 Compound Name M7824 Phase 2 [18]
MOA Inhibitor
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 Compound Name BGB-A333 Phase 1/2 [19]
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 Compound Name GS-4224 Phase 1/2 [20]
Synonyms
Methyl Pyridazine-4-carboxylate; 34231-77-1; PYRIDAZINE-4-CARBOXYLIC ACID METHYL ESTER; 4-PYRIDAZINECARBOXYLIC ACID, METHYL ESTER; MFCD09953488; ACMC-1AJNN; methyl 4-pyridazinecarboxylate; methylpyridazine-4-carboxylate; SCHEMBL1421640; DTXSID30498310; AMY24958; BCP22435; ANW-50355; ZINC12359421; AKOS015854403; Methyl pyridazine-4-carboxylate, 97%; AC-4414; CS-W003697; PB31452; 4-Pyridazinecarboxylic acid methyl ester; AK-48857; SY004472; AB0024323; DB-030309; FT-0717698; W5569; S-2990; J-522632
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MOA Inhibitor
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 Compound Name NM21-1480 Phase 1/2 [21]
MOA Modulator
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 Compound Name LY3300054 Phase 1 [18]
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 Compound Name MSB2311 Phase 1 [14]
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 Compound Name Anti-PD-L1 Phase 1 [22]
Synonyms
BMS-936559
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 Compound Name FAZ053 Phase 1 [15]
MOA Inhibitor
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 Compound Name Anti-PD-L1 CSR T cells Phase 1 [23]
MOA CAR-T-Cell-Therapy
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 Compound Name BMS-986189 Phase 1 [14]
MOA Inhibitor
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 Compound Name Cosibelimab Phase 1 [24]
Synonyms
CK-301/TG-1501
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 Compound Name CA-170 Phase 1 [25]
MOA Inhibitor
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 Compound Name PD-L1 t-haNK Phase 1 [26]
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 Compound Name KD033 Phase 1 [27]
MOA Inhibitor
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 Compound Name C-Met/PD-L1 CAR-T Cell Phase 1 [28]
MOA CAR-T-Cell-Therapy(Dual specific)
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 Compound Name CA-170 Phase 1 [18]
Synonyms
3-Aminopyrrolidine dihydrochloride; 103831-11-4; pyrrolidin-3-amine dihydrochloride; 3-Pyrrolidinamine, dihydrochloride; 3-Aminopyrrolidine 2HCl; 3-Aminopyrrolidine diHCl; SCHEMBL555933; ACMC-2099s1; ACMC-2099s3; ACMC-20989g; 3-pyrrolidinamine dihydrochloride; CTK0H7226; DTXSID00583661; MolPort-002-343-989; NJPNCMOUEXEGBL-UHFFFAOYSA-N; 3-Amino-pyrrolidine dihydrochloride; KS-00000JI6; ACT01710; ANW-14978; SBB003982; ( -3-Aminopyrrolidine dihydrochloride; AKOS015844825; VP60158; AM85320; VP60228; TRA0055207; TRA0000843; TRA0097
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MOA Inhibitor
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 Compound Name FS118 Phase 1 [14]
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 Compound Name PF-07257876 Phase 1 [29]
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 Compound Name MCLA-145 Phase 1 [30]
MOA Agonist
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 Compound Name GEN1046 Phase 1 [31]
MOA Agonist
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 Compound Name ALPN-202 Phase 1 [32]
MOA Inhibitor
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 Compound Name TAK-252 Phase 1 [33]
Synonyms
SL-279252
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MOA Agonist
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 Compound Name INBRX-105 Phase 1 [34]
MOA Inhibitor
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 Compound Name LY3415244 Phase 1 [35]
MOA Inhibitor
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 Compound Name A337 Phase 1 [11]
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 Compound Name IBI318 Phase 1 [36]
MOA Inhibitor
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 Compound Name PMID30107136-Compound-Example2 Patented [37]
MOA Inhibitor
Activity IC50 = 150 nM
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 Compound Name PMID30107136-Compound-Example1 Patented [37]
MOA Inhibitor
Activity IC50 = 18 nM
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 Compound Name PMID30247903-Compound-General structure7 Investigative [14]
Synonyms
PMID30247903Compound7
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MOA Inhibitor
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 Compound Name CA-327 Investigative [14]
MOA Inhibitor
External Link
 Compound Name PMID30247903-Compound-General structure8 Investigative [14]
Synonyms
PMID30247903Compound8
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MOA Inhibitor
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 Compound Name PMID30247903-Compound-General structure5 Investigative [14]
Synonyms
PMID30247903Compound5
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MOA Inhibitor
External Link
 Compound Name PMID30247903-Compound-General structure12 Investigative [14]
Synonyms
PMID30247903Compound12
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MOA Inhibitor
External Link
 Compound Name PMID30247903-Compound-General structure9 Investigative [14]
Synonyms
PMID30247903Compound9
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MOA Inhibitor
External Link
 Compound Name PMID30247903-Compound-General structure6 Investigative [14]
Synonyms
PMID30247903Compound6
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MOA Inhibitor
External Link
 Compound Name PMID30247903-Compound-General structure10 Investigative [14]
Synonyms
PMID30247903Compound10
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MOA Inhibitor
External Link
 Compound Name YH011 Investigative [38]
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 Compound Name YH010 Investigative [39]
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 Compound Name RG6084 Phase 1 [40]
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2C10: Pancreatic cancer 182 Compound(s) Regulating the Disease Click to Show/Hide the Full List
 Compound Name Atezolizumab Approved [18]
External Link
 Compound Name Trimethadione Approved [41]
Synonyms
Absentol; Absetil; Convenixa; Convexina; Edion; Epidione; Epidone; Epixal; Etydion; Minoaleuiatin; Minoaleviatin; Petidion; Petidon; Petilep; Petimalin; Pitmal; Ptimal; Tioxanona; Tredione; Tricione; Tridilona; Tridion; Tridione; Tridone; Trilidona; Trimedal; Trimedone; Trimetadiona; Trimetadione; Trimethadion; Trimethadionum; Trimethdione; Trimethin; Trimethinum; Trimetin; Trioksal; Trioxanona; Triozanona; Tromedone; Troxidone; Abbott Brand of Trimethadione; Trimetadione [DCIT]; A 2297; Mino-Aleviatin; Neo-Absentol; Tridione (TN); Trimetadiona [INN-Spanish]; Trimethadione [INN:JAN]; Trimethadionum [INN-Latin]; Trimethadione (JP15/INN); 3,3,5-Trimethyl-2,4-diketooxazolidine; 3,5,5,-Trimethyloxazolidine-2,4-dione; 3,5,5-TRIMETHYL-OXAZOLIDINE-2,4-DIONE; 3,5,5-Trimethyl-1,3-oxazolidine-2,4-dione; 3,5,5-Trimethyl-2,4-oxazolidinedione; 3,5,5-Trojmetylooksazolidyno-2,4-dion; 3,5,5-Trojmetylooksazolidyno-2,4-dion [Polish]
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 Compound Name Motixafortide Approved [18]
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 Compound Name Uridine triacetate Approved [42]
Synonyms
PN401
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External Link
 Compound Name Bentiromide Approved [43]
Synonyms
Bentiromide sodium; 41748-47-4; N-Benzoyl-L-tyrosyl-4-aminobenzoic acid sodium salt; NCGC00164607-01; EINECS 255-530-7; DSSTox_CID_26476; DSSTox_RID_81647; DSSTox_GSID_46476; DTXSID6046476; CHEMBL3188891; Tox21_112229; AKOS024373587; ACM41748474; Sodium (S)-4-((2-(benzoylamino)-3-(4-hydroxyphenyl)-1-oxopropyl)amino)benzoate; CAS-41748-47-4; FT-0771579; ST51012404; N-Benzoyl-L-tyrosine p-amidobenzoic acid sodium salt; sodium (S)-4-(2-benzamido-3-(4-hydroxyphenyl)propanamido)benzoate; N-Benzoyl-L-tyrosine p-amidobenzoic acid so
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External Link
 Compound Name Olaparib Approved [18]
Synonyms
AZD 2281; AZD2281; AZD-2281; Acylpiperazine analogue, 47; KU-0059436; KU-59436; Olaparib, KU-0059436, AZD2281,KU0059436, AZD2281; 4-[(3-{[4-Cyclopropylcarbonyl)piperazin-4-yl]carbonyl}-4-fluorophenyl)methyl]phtalazin-1(2H)-one; 4-[3-(4-Cyclopropanecarbonyl-piperazine-1-carbonyl)-4-fluoro-benzyl]-2H-phthalazin-1-one
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External Link
 Compound Name Streptozocin Approved [44]
Synonyms
Estreptozocina; STREPTOZOTOCIN; STRZ; Streptozocine; Streptozocinium; Streptozocinum; Streptozosin; Zanosar; Alkylating agent; Binds to DNA; Streptozocinium [Latin]; Streptozocine [INN-French]; Streptozocinum [INN-Latin]; Zanosar (TN); Streptozocin (USAN/INN); Streptozocin, Zanosar, STZ,Streptozotocin;N-(Methylnitrosocarbamoyl)-alpha-D-glucosamine; N-D-Glucosyl-(2)-N'-nitrosomethylharnstoff; N-D-Glucosyl-(2)-N'-nitrosomethylurea; D-Glucose, 2-deoxy-2-(((methylnitrosoamino)carbonyl)amino)-(9CI); 1-methyl-1-nitroso-3-[(2S,3R,4R,5S,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]urea; 2-Deoxy-2-(((methylnitrosoamino)carbonyl)amino)-D-glucopyranose; 2-Deoxy-2-(3-methyl-3-nitrosoureido)-D-glucopyranose; 2-Deoxy-2[[(methylnitrosoamino)-carbonyl]amino]-D-glucopyranose; 2-deoxy-2-{[methyl(nitroso)carbamoyl]amino}-alpha-D-glucopyranose
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External Link
 Compound Name Plazomicin Phase 3 [45]
Synonyms
ACHN-490; UNII-LYO9XZ250J; 1154757-24-0; LYO9XZ250J; Plazomicin [USAN:INN]; Plazomicin (USAN); ZINC68150640; DB12615; D10151; D-Streptamine,
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External Link
 Compound Name Taxol Approved [18]
Synonyms
C47H51NO14; weekly paclitaxel; Micellar Paclitaxel; Paclitaxel [USAN:INN:BAN]; SCHEMBL15000506; Benzenepropanoic acid, beta-(benzoylamino)-alpha-hydroxy-, 6,12b-bis(acetyloxy)-12-(benzoyloxy)-2a,3,4,4a,5,6,9,10,11,12,12a,12b-dodecahydro-4,11-dihydroxy-4a,8,13,13-tetramethyl-5-oxo-7,11-methano-1H-cyclodeca(3,4)benz(1,2-b)oxet-9-yl ester, (2aR-(2aalpha,4beta,4abeta,6beta,9alpha(alphaR*,betaS*),11alpha,12alpha,12aalpha,12balpha))-
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 Compound Name Ibrutinib Phase 3 [18]
Synonyms
PCI-32765; Ibrutinib (BTK inhibitor)
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External Link
 Compound Name Erlotinib Approved [46]
Synonyms
Erlotinin; Tarceva; Erlotinib Base; OSI 744; R 1415; CP 358,774; CP-358774; Erlotinib(Tarceva); Tarceva (TN); CP-358,774; Erlotinib, OS-774; N-(3-ethynylphenyl)[6,7-bis(2-methoxyethoxy)quinazolin-4-yl]amine; N-(3-Ethynylphenyl)-6,7-bis(2-methoxyethoxy)-4-quinazolinamine; N-(3-Ethynylphenyl)-6,7-bis(2-methoxyethoxy)quinazolin-4-amine; [6,7-BIS(2-METHOXY-ETHOXY)QUINAZOLINE-4-YL]-(3-ETHYNYLPHENYL)AMINE; [6,7-Bis-(2-methoxy-ethoxy)-quinazolin-4-yl]-(3-ethynyl-phenyl)-amine; 4-[(3-Ethynylphenyl)amino]-6,7-bis(2-methoxyethoxy)quinazoline
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External Link
 Compound Name Ruxolitinib Approved [47]
Synonyms
Ruxolitinib (JAK inhibitor)
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 Compound Name Nivolumab Approved [18]
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 Compound Name Coenzyme Q10 Phase 2 [18]
Synonyms
CoQ10; Coenzyme Q10 (oral formulation); CoQ10 platform technology, Ryan (Receptagen); Coenzyme Q10 (oral formulation), Receptagen
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 Compound Name Aglatimagene besadenovec Phase 1/2 [18]
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 Compound Name Zolbetuximab Phase 3 [48]
Synonyms
IMAB362
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External Link
 Compound Name AC-1204 Phase 3 [49]
Synonyms
isoindoline hydrochloride; 32372-82-0; 2,3-Dihydroisoindole hydrochloride; 2,3-dihydro-1H-isoindole hydrochloride; 2,3-Dihydro-1H-isoindole HCl; Isoindoline HCl salt; 1H-Isoindole, 2,3-dihydro-, hydrochloride; Isoindoline hydrochloride, 97%; Isoindolinehydrochloride; Isoindoline, HCl; ISOINDOLINE HCL; AC1Q38WR; dihydroisoindole hydrochloride; KSC491I3F; AMBZ0192; SCHEMBL4702076; CTK3J1432; DTXSID50487241; MolPort-003-986-749; NOVIRODZMIZUPA-UHFFFAOYSA-N; BH168; CS-D1516; ACT08858; ACN-S003258; KS-000001RA
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 Compound Name Radiosensitizer gene therapy Phase 3 [50]
Synonyms
Radiosensitizer gene therapy (prostate cancer)
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 Compound Name Glufosfomide Phase 3 [51]
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 Compound Name Yttrium (90Y) clivatuzumab tetraxetan Phase 3 [52]
Synonyms
PAM4 mAb; Yttrium Y 90 clivatuzumab tetraxetan; Anti-MUC1 PAM4 monoclonal antibody; Clivatuzumab tetraxetan-[90Y]; HPAM4-Cide; IMMU-107; PAM-4; PAM4-Y-90; Yttrium-90-hPAM4; 90Y-clivatuzumab tetraxetan; 90Y-hPAM4
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 Compound Name Y-90 Clivatuzumab Phase 3 [53]
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 Compound Name Civacir Phase 3 [54]
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 Compound Name GV1001 Phase 3 [55]
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 Compound Name Masitinib Phase 3 [18]
Synonyms
790299-79-5; AB1010; Masatinib; Masitinib (AB1010); Masivet; AB-1010; AB 1010; UNII-M59NC4E26P; Masitinib [INN]; M59NC4E26P; 4-[(4-Methyl-1-piperazinyl)methyl]-N-[4-methyl-3-[[4-(3-pyridinyl)-2-thiazolyl]amino]phenyl]benzamide; CHEMBL1908391; CHEBI:63450; Masitinib (INN); N-(4-Methyl-3-((4-(pyridin-3-yl)thiazol-2-yl)amino)phenyl)-4-((4-methylpiperazin-1-yl)methyl)benzamide; Q-201339; C28H30N6OS; N-(4-methyl-3-(4-(pyridin-3-yl)thiazol-2-ylamino)phenyl)-4-((4-methylpiperazin-1-yl)methyl)benzamide
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External Link
 Compound Name Glufosfamide Phase 3 [18]
Synonyms
Glucosylifostamide mustard; D 19575; D-19575; Glc-IPM; Glucosyl-ifosfamide mustard; Beta-D-Glucopyranose 1-(N,N'-bis(2-chloroethyl)phosphorodiamidate; Beta-D-Glucopyranose, 1-(N,N'-bis(2-chloroethyl)phosphorodiamidate); (2S,3R,4S,5S,6R)-2-bis(2-chloroethylamino)phosphoryloxy-6-(hydroxymethyl)oxane-3,4,5-triol
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 Compound Name Sapacitabine Phase 3 [18]
Synonyms
CYC682
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 Compound Name Pelareorep Phase 2 [15]
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 Compound Name Pamrevlumab Phase 3 [56]
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 Compound Name GRASPA Phase 1 [57]
Synonyms
L-asparaginase (erythrocyte-encapsulated, acute lymphoblastic leukemia/solid tumor), ERYtech
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 Compound Name Pancreas algenpantucel-L Phase 3 [58]
Synonyms
HyperAcute (TN)
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External Link
 Compound Name CPI-613 Phase 3 [59]
Synonyms
95809-78-2; 6,8-bis(benzylthio)octanoic acid; CPI 613; MLS006010202; SCHEMBL1062218; 6,8-Bis(benzylsulfanyl)octanoic acid; Octanoic acid, 6,8-bis((phenylmethyl)thio)-; Octanoic acid, 6,8-bis[(phenylMethyl)thio]-; 6,8-Bis[(phenylmethyl)thio]octanoic acid; CPI613; CHEMBL3186849; QCR-193; AOB1058; MolPort-023-219-128; HMS3656L06; C22H28O2S2; BCP04663; EX-A2043; s2776; AKOS025142095; BCP9000552; DB12109; RL06062; CS-0961; NCGC00344764-01; SMR004701300; AS-16613; BC261916; AK174899; HY-15453; BCP0726000030; KB-293127; AB0035874
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External Link
 Compound Name Zarnestra Phase 3 [60]
Synonyms
JAN; Tipifarnib; Tipifarnib [USAN]; R 115777; R115777; R-11577; R-115777; Tipifarnib (USAN/INN); Zarnestra, IND 58359, R115777, Tipifarnib; (R)-6-(Amino(4-chlorophenyl)(1-methyl-1H-imidazol-5-yl)methyl)-4-(3-chlorophenyl)-1-methyl-2(1H)-quinolinone; (R)-R115777; 2 (1H))-Quinolinone,6-(amino(4-chlorophenyl)(1-methyl-1H-imidazol-5-yl)methyl)-4-(3-chlorophenyl)-1-methyl-, 2(1H)-quinolinone; 6-[(R)-amino(4-chlorophenyl)(1-methyl-1H-imidazol-5-yl)methyl]-4-(3-chlorophenyl)-1-methylquinolin-2(1H)-one; 6-[(R)-amino-(4-chlorophenyl)-(3-methylimidazol-4-yl)methyl]-4-(3-chlorophenyl)-1-methylquinolin-2-one; 6-[(S)-AMINO(4-CHLOROPHENYL)(1-METHYL-1H-IMIDAZOL-5-YL)METHYL]-4-(3-CHLOROPHENYL)-1-METHYLQUINOLIN-2(1H)-ONE
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 Compound Name MM-398 Phase 3 [61]
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 Compound Name Marimastat Phase 3 [62]
Synonyms
Marimastat [USAN]; BB 2516; BB-2516; Marimastat (USAN/INN); (2R,3S)-N-[(2S)-3,3-dimethyl-1-(methylamino)-1-oxobutan-2-yl]-N',3-dihydroxy-2-(2-methylpropyl)butanediamide; (2S,3R)-3-(((1S)-2,2-Dimethyl-1-(methylcarbamoxy)propyl)carboyl)-2-hydroxy-5-methylhexanohydroxamic acid; (2S,3R)-3-(((1S)-2,2-Dimethyl-1-(methylcarbamoyl)propyl)carbamoyl)-2-hydroxy-5-methylhexanohydroxamic acid; (2S,3R)-N(4)-[(2S)-3,3-dimethyl-1-(methylamino)-1-oxobutan-2-yl]-N(1),2-dihydroxy-3-(2-methylpropyl)butanediamide
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 Compound Name AM0010 Phase 3 [63]
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 Compound Name ANX-510 Phase 3 [64]
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 Compound Name Napabucasin Phase 3 [18]
Synonyms
83280-65-3; UNII-Z1HHM49K7O; 2-acetylnaphtho[2,3-b]furan-4,9-dione; Z1HHM49K7O; 2-Acetylnaphtho(2,3-b)furan-4,9-dione; 2-Acetyl-4H,9H-naphtho[2,3-b]furan-4,9-dione; Napabucasin [USAN:INN]; Napabucasin (BBI608); 2-Acetylfuranonaphthoquinone; CHEMBL64130; Napabucasin (JAN/USAN/INN); SCHEMBL1883845; Napabucasin - BBI 608/ FNQ; 2-Acetylfuro-1,4-naphthoquinone; DPHUWDIXHNQOSY-UHFFFAOYSA-N; MolPort-039-101-321; EX-A1314; ZINC13306865; s7977; AKOS027470201; DB12155; CS-1747; ACN-053294; HY-13919
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 Compound Name Algenpantucel-L Phase 3 [65]
Synonyms
HyperAcute pancreas (TN)
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 Compound Name OT-101 Phase 2/3 [18]
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 Compound Name RP101 Phase 2/3 [66]
Synonyms
SCHEMBL15589316; CHEMBL3703295; BDBM149820; US8975415,
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External Link
 Compound Name NLG8189 Phase 2/3 [18]
Synonyms
1-Methyl-D-tryptophan; Indoximod; 110117-83-4; D-Tryptophan, 1-methyl-; D-1MT; Indoximod (NLG-8189); D-1-methyltryptophan; UNII-TX5CYN1KMZ; D-(+)-1-Methyltryptophan; TX5CYN1KMZ; (R)-2-amino-3-(1-methyl-1H-indol-3-yl)propanoic acid; (2R)-2-amino-3-(1-methylindol-3-yl)propanoic acid; NSC-721782; (2R)-2-amino-3-(1-methyl-3-indolyl)propanoic acid; 1-MT; (2R)-2-azanyl-3-(1-methylindol-3-yl)propanoic acid; (2R)-2-amino-3-(1-methyl-1H-indol-3-yl)propanoic acid; D-l-Methyltryptophan; Indoximod [USAN:INN]; NLG-8189; NLG 8189
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External Link
 Compound Name LY2157299 Phase 2/3 [18]
Synonyms
Galunisertib; 700874-72-2; LY 2157299; LY-2157299; UNII-3OKH1W5LZE; 4-(2-(6-methylpyridin-2-yl)-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazol-3-yl)quinoline-6-carboxamide; 3OKH1W5LZE; Galunisertib (LY2157299); AK-79916; 4-[5,6-Dihydro-2-(6-methyl-2-pyridinyl)-4H-pyrrolo[1,2-b]pyrazol-3-yl]-6-quinolinecarboxamide; 4-(2-(6-Methylpyridin-2-yl)-5,6-dihydro-4H-pyrrolo-[1,2-b]pyrazol-3-yl)quinoline-6-carboxamide; 4-[2-(6-methylpyridin-2-yl)-4H,5H,6H-pyrrolo[1,2-b]pyrazol-3-yl]quinoline-6-carboxamide
    Click to Show/Hide
External Link
 Compound Name SM-88 Phase 2/3 [67]
External Link
 Compound Name SiG12D-LODER Phase 2 [18]
External Link
 Compound Name BNT141 Phase 2 [68]
External Link
 Compound Name BNT321 Phase 2 [69]
Synonyms
MVT-5873
    Click to Show/Hide
External Link
 Compound Name BPM 31510 Phase 2 [70]
External Link
 Compound Name GC4711 Phase 2 [71]
Synonyms
UNII-FW5T90VM32; FW5T90VM32; GC-4419 dipropionate; Bis-propionato(gc4419); Avasopasem manganese dipropionate; GC-4711; 2248030-85-3; Manganese(II), bis-propionato((4aS,13aS,17aS,21aS)-1,2,3,4,4a,5,6,12,13,13a,14,15,16,17,17a,18,19,20,21,21a-eicosahydro-11,7-nitrilo-7H-dibenzo(b,H)(1,4,7,10)tetraaza-cycloheptadecine-kn5,kn13,kn18,kn21,kn22)-,
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External Link
 Compound Name CYTO-401 Phase 2 [72]
External Link
 Compound Name Zenocutuzumab Phase 2 [73]
External Link
 Compound Name Cabiralizumab Phase 2 [18]
External Link
 Compound Name VS-6063 Phase 2 [18]
Synonyms
Defactinib hydrochloride; 1073160-26-5; Defactinib (hydrochloride); UNII-L2S469LM49; Defactinib hydrochloride [USAN]; L2S469LM49; Defactinib hydrochloride (USAN); Benzamide, N-methyl-4-[[4-[[[3-[methyl(methylsulfonyl)amino]-2-pyrazinyl]methyl]amino]-5-(trifluoromethyl)-2-pyrimidinyl]amino]-, hydrochloride; Defactinib HCl; Benzamide, N-methyl-4-((4-(((3-(methyl(methylsulfonyl)amino)-2-pyrazinyl)methyl)amino)-5-(trifluoromethyl)-2-pyrimidinyl)amino)-, hydrochloride (1:1); Benzamide, N-methyl-4-[[4-[[[3-[methyl(methylsu
    Click to Show/Hide
External Link
 Compound Name MENK Phase 2 [51]
External Link
 Compound Name CO-101 Phase 2 [74]
Synonyms
methyl 2-(dimethylcarbamoyl)benzoate; 26593-43-1; Phthalamic acid, N,N-dimethyl-, methyl ester; CO 101; BRN 2504723; N,N-Dimethylphthalamic acid methyl ester; N,N-Dimethylphthalamic acid, methyl ester; AC1Q5ZAU; 2-09-00-00601 (Beilstein Handbook Reference); AC1L4V19; CTK4F8203; DTXSID50181156; 2-methoxycarbonyl-N,N-dimethylbenzamide; LS-109082; Benzoic acid,2-[(dimethylamino)carbonyl]-, methyl ester
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External Link
 Compound Name MENK Phase 2 [18]
Synonyms
IRT-101
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External Link
 Compound Name TL-118 Phase 2 [75]
Synonyms
Hamsa 1; TL-111; TL-112; Combination anti-angiogenic therapy (oral suspension, solid tumors), Tiltan Pharma
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External Link
 Compound Name Antroquinonol Phase 2 [18]
Synonyms
Hocena; Fungal extract (cancer), Golden Biotechnology
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 Compound Name NPC-1C Phase 2 [18]
Synonyms
Ensituximab
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External Link
 Compound Name Necuparanib Phase 2 [76]
External Link
 Compound Name CCX872 Phase 2 [18]
External Link
 Compound Name GC4419 Phase 1/2 [18]
Synonyms
Avasopasem manganese; UNII-EY1WA413UL; EY1WA413UL; Avasopasem manganese [USAN]; SC-72325A; M-40419; 435327-40-5; Manganese, dichloro((4aS,13aS,17aS,21aS)-1,2,3,4,4a,5,6,12,13,13a,14,15,16,17,17a,18,19,20,21,21a-eicosahydro-7,11-nitrilo-7H-dibenzo(b,H)-5,13,18,21-tetraazacycloheptadecine-kappaN5,kappaN13,kappaN18,kappaN21,kappaN22)-, (pb-7-11-2344'3')-
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External Link
 Compound Name Istiratumab Phase 2 [15]
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 Compound Name GI-4000 Phase 2 [77]
External Link
 Compound Name OCV-101 Phase 2 [78]
Synonyms
OTS-11101
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External Link
 Compound Name RX-3117 Phase 2 [18]
Synonyms
Antimetabolite (cancer), Rexahn; Antimetabolite (cancer), Rexahn/ Teva
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External Link
 Compound Name Ensitiximab Phase 2 [51]
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 Compound Name GI-4000 + gemcitabine Phase 2 [79]
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 Compound Name BC-819 Phase 2 [80]
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 Compound Name IRT-102 Phase 2 [81]
External Link
 Compound Name LE-DT Phase 2 [82]
Synonyms
Liposomal docetaxel
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External Link
 Compound Name TH-302 Phase 2 [18]
Synonyms
evofosfamide; 918633-87-1; TH 302; TH302; UNII-8A9RZ3HN8W; Evofosfamide(TH 302); n,n'-bis(2-bromoethyl)phosphorodiamidic acid (1-methyl-2-nitro-1h-imidazol-5-yl)methyl ester; 8A9RZ3HN8W; compound 3b; Evofosfamide;HAP-302; Phosphorodiamidic acid, N,N'-bis(2-bromoethyl)-, (1-methyl-2-nitro-1H-imidazol-5-yl)methyl ester; 2-bromo-N-[(2-bromoethylamino)-[(3-methyl-2-nitroimidazol-4-yl)methoxy]phosphoryl]ethanamine; Evofosfamide [USAN:INN]; Evofosfamide(TH-302); C9H16Br2N5O4P; CHEMBL260046; SCHEMBL2357174
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External Link
 Compound Name Demcizumab Phase 2 [51]
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 Compound Name Anti-PSCA mab Phase 2 [83]
External Link
 Compound Name ALT-803 Phase 2 [15]
Synonyms
IL-15 agonist/ IL-15R alpha-Fc fusion complex (cancer), Altor BioScience
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External Link
 Compound Name ARQ 761 Phase 2 [18]
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 Compound Name Reolysinpelareorep Phase 2 [18]
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 Compound Name PBI-05204 Phase 2 [18]
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 Compound Name PCI-27483 Phase 2 [84]
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 Compound Name RX-0201 Phase 2 [51]
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 Compound Name CP-613 Phase 2 [85]
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 Compound Name CART 19 Preclinical [86]
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 Compound Name VT-122 Phase 1 [51]
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 Compound Name PEGPH20 Phase 2 [87]
External Link
 Compound Name Ficlatuzumab Phase 2 [18]
Synonyms
AV-299
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External Link
 Compound Name Tigatuzumab Phase 2 [88]
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 Compound Name CRS-207 Phase 2 [89]
External Link
 Compound Name CAP1-6D Phase 2 [90]
Synonyms
Modified CEA peptide (pancreatic cancer), University of Chicago
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External Link
 Compound Name SGT-53 Phase 2 [18]
Synonyms
P53 gene stimulator (solid tumor), Synergene Therapeutics
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External Link
 Compound Name Tarextumab Phase 2 [91]
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 Compound Name BVD-523 Phase 2 [18]
External Link
 Compound Name Ocaperidone Phase 2 [15]
Synonyms
Ocaperidona; 129029-23-8; UNII-26HUS7139V; 3-(2-(4-(6-Fluoro-1,2-benzisoxazol-3-yl)piperidino)ethyl)-2,9-dimethyl-4H-pyrido(1,2-a)pyrimidin-4-one; 26HUS7139V; Ocaperidonum; Ocaperidonum [INN-Latin]; Ocaperidona [INN-Spanish]; 4H-Pyrido[1,2-a]pyrimidin-4-one,3-[2-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]ethyl]-2,9-dimethyl-; Ocaperidone (USAN); Ocaperidone [USAN:INN:BAN]; 3-[2-[4-(6-Fluorobenzo[d]isoxazol-3-yl)piperidin-1-yl]ethyl]-2,9-dimethyl-4H-pyrido[1,2-a]pyrimidin-4-one; 3-[2-[4-(6-fluoro-1,2-benzoxazol-3-yl)piperidin-1-yl]ethyl]-2,9-dimethylpyrido[1,2-a]pyrimidin-4-one; 8-[2-[4-(6-fluorobenzo[d]isoxazol-3-yl)-1-piperidyl]ethyl]-2,9-dimethyl-6,10-diazabicyclo[440]deca-2,4,8,10-tetraen-7-one; FG-3019
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External Link
 Compound Name Encapsulated live cells converting ifosfamide Phase 2 [18]
External Link
 Compound Name LY2603618 Phase 2 [92]
Synonyms
Rabusertib; 911222-45-2; LY 2603618; LY-2603618; UNII-3S9L1NU6U7; 3S9L1NU6U7; IC-83; ly2603618 IC-83; (S)-1-(5-bromo-4-methyl-2-(morpholin-2-ylmethoxy)phenyl)-3-(5-methylpyrazin-2-yl)urea; n-(5-bromo-4-methyl-2-((2s)-2-morpholinylmethoxy)phenyl)-n'-(5-methyl-2-pyrazinyl)urea; LY2603618 (IC-83); Rabusertib [USAN:INN]; 3-(5-Bromo-4-methyl-2-[(2s)-morpholin-2-ylmethoxy]phenyl)-1-(5-methylpyrazin-2-yl)urea; N-[5-Bromo-4-methyl-2-[(2S)-2-morpholinylmethoxy)phenyl]-N'-(5-methyl-2-pyrazinyl)urea
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External Link
 Compound Name Salirasib Discontinued in Phase 1/2 [93]
Synonyms
162520-00-5; Farnesylthiosalicylic acid; S-Farnesylthiosalicylic acid; UNII-MZH0OM550M; MZH0OM550M; CHEMBL23293; AK186909; Farnesyl Thiosalicylic Acid; 2-[[(2E,6E)-3,7,11-Trimethyl-2,6,10-dodecatrien-1-yl]thio]benzoic Acid; 2-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl]sulfanylbenzoic acid; 2-((2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienylthio)benzoic acid; 2-(((2E,6E)-3,7,11-Trimethyl-2,6,10-dodecatrienyl)sulfanyl)benzoic acid; Benzoic acid, 2-(((2E,6E)-3,7,11-trimethyl-2,6,10-dodecatrienyl)thio)-; FTS; Farnesylthiosalicyclic acid; FTS, Thyreos; Ras antagonists, Thyreos; S-trans; Th-101; Trans-farnesylthiosalicylicacid; FTS (oral, cancer), Concordia; Farnesylthiosalicyclic acid (oral, cancer), Concordia; Ras-inhibitors (cancer), Concordia; FTS (oral, cancer), Concordia/Ono; KD032
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External Link
 Compound Name MM-141 Phase 2 [18]
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 Compound Name GB1275 Phase 1/2 [94]
External Link
 Compound Name ABTL0812 Phase 1/2 [95]
Synonyms
(9Z,12Z)-2-Hydroxy-9,12-octadecadienoic acid; (9Z,12Z)-2-hydroxyoctadeca-9,12-dienoic acid; (9Z,12Z)-2-hydroxyoctadecadienoic acid; (alpha)-Hydroxylinoleic acid; .ALPHA.-HYDROXYLINOLEIC ACID; 0DE74TJ7EZ; 2-hydroxy-9Z,12Z-Octadecadienoic acid; 2-hydroxylinoleic acid; 57818-44-7; 9,12-Octadecadienoic acid, 2-hydroxy-, (9Z,12Z)-; 9,12-Octadecadienoic acid, 2-hydroxy-, (Z,Z)-; ABTL0812; ABTL-0812; a-Hydroxylinoleic acid; AKOS040740632; alpha-Hydroxylinoleic acid; CHEBI:136927; CS-7178; DTXSID301258077; hydroxylinoleic acid; HY-U00141; LMFA02000290; MS-24253; s9611; SCHEMBL320069; UNII-0DE74TJ7EZ
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 Compound Name GP-2250 Phase 1/2 [96]
External Link
 Compound Name Delolimogene mupadenorepvec Phase 1/2 [97]
Synonyms
LOAd703
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External Link
 Compound Name GSK3145095 Phase 1/2 [98]
Synonyms
1622849-43-7; CHEMBL4452233; (S)-5-benzyl-N-(7,9-difluoro-2-oxo-2,3,4,5-tetrahydro-1H-benzo[b]azepin-3-yl)-4H-1,2,4-triazole-3-carboxamide; UNII-B4D3WPS7JY; B4D3WPS7JY; SCHEMBL17312826; BCP31015; EX-A3069; BDBM50502339; s8845; GSK-3145095; HY-111946; CS-0094287; GSK 3145095; FC1=CC2=C(NC(=O)[C@H](CC2)NC(=O)C2=NN=C(CC3=CC=CC=C3)N2)C(F)=C1; (S)-5-Benzyl-N-(7,9-difluoro-2-oxo-2,3,4,5-tetrahydro-1hbenzo(b)azepin-3-yl)-1H-1,2,4-triazole-3-carboxamide (7,7-dimethyl-2- oxobicyclo(2.2.1)heptan-1-yl)
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 Compound Name Encapsulated cell therapy Phase 1/2 [99]
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 Compound Name ETBX-011 cancer vaccine Phase 1/2 [77]
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 Compound Name BPX-601 Phase 1/2 [100]
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 Compound Name NANT Phase 1/2 [18]
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 Compound Name BrevaRex Phase 1/2 [101]
Synonyms
BrevaRex MAb; monoclonal antibody
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External Link
 Compound Name DCVax-Pancreas Phase 1/2 [102]
Synonyms
Dendritic cell-based immunotherapy (pancreatic cancer), Northwest Biotherapeutics
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External Link
 Compound Name PEGylated hyaluronidase (human recombinant) Phase 1/2 [103]
Synonyms
PEGylated hyaluronidase; PEGylated hyaluronidase (human recombinant) (intravenous, stroke/cancer), Halozyme
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External Link
 Compound Name CAR-T cells targeting mesothelin Phase 1/2 [104]
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 Compound Name MALP-2S Phase 1/2 [105]
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 Compound Name Anti-Mesothelin CAR-T cells Phase 1/2 [106]
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 Compound Name Anti-MUC1 CAR T Cells Phase 1/2 [107]
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 Compound Name Anti-HER2 CAR-T Phase 1/2 [108]
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 Compound Name CAR-T Cells targeting EpCAM Phase 1/2 [109]
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 Compound Name Anti-MUC1 AR20.5 Phase 1/2 [15]
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 Compound Name AR20.5 Phase 1/2 [18]
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 Compound Name G0-203-2c Phase 1/2 [110]
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 Compound Name LOAd703 Phase 1/2 [18]
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 Compound Name Anti-mesothelin CAR transduced PBL Phase 1/2 [111]
External Link
 Compound Name M9241 Phase 1 [112]
Synonyms
NHS-IL12
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External Link
 Compound Name NBF-006 Phase 1 [113]
External Link
 Compound Name AB680 Phase 1 [114]
Synonyms
AB-680; UNII-J6K8WSV73A; J6K8WSV73A; CHEMBL4471306; 2105904-82-1; (((((2R,3S,4R,5R)-5-(6-chloro-4-(((S)-1-(2-fluorophenyl)ethyl)amino)-1H-pyrazolo[3,4-b]pyridin-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)(hydroxy)phosphoryl)methyl)phosphonic acid; [[(2~{R},3~{S},4~{R},5~{R})-5-[6-chloranyl-4-[[(1~{S})-1-(2-fluorophenyl)ethyl]amino]pyrazolo[3,4-b]pyridin-1-yl]-3,4-bis(oxidanyl)oxolan-2-yl]methoxy-oxidanyl-phosphoryl]methylphosphonic acid; SCHEMBL19100484; GTPL10707; BDBM50527134; HY-125286; CS-0090231; [[(2R,3S,4R,5R)-5-[6-chloro-4-[[(1S)-1-(2-fluorophenyl)ethyl]amino]pyrazolo[3,4-b]pyridin-1-yl]-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl]methylphosphonic acid; QDH
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External Link
 Compound Name STAT400 Phase 1 [115]
External Link
 Compound Name CEND-1 Phase 1 [116]
Synonyms
iRGD; UNII-Z8MXU5GH4Q; Z8MXU5GH4Q; iRGD-peptide; 1392278-76-0; Internalized-arginylglycylaspartic acid cyclic peptide; Q48988348; L-Cysteine, L-cysteinyl-L-arginylglycyl-L-alpha-aspartyl-L-lysylglycyl-L-prolyl-L-alpha-aspartyl-, cyclic (1->9)-disulfide
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External Link
 Compound Name CAR-T Cells targeting EGFRvIII Phase 1 [117]
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 Compound Name HuCART-meso cells Phase 1 [118]
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 Compound Name OCV-105 Phase 1 [119]
Synonyms
Cancer vaccine (pancreas), Otsuka/OncoTherapy
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External Link
 Compound Name SBP-101 Phase 1 [51]
Synonyms
diethyl dihydroxyhomospermine
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External Link
 Compound Name RG7882 Phase 1 [15]
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 Compound Name CART-meso-19 T cells Phase 1 [120]
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 Compound Name MOv19-BBz CAR T cells Phase 1 [121]
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 Compound Name Anti-MUC1 AR20.5 mab Phase 1 [122]
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 Compound Name Anti-CEA-CAR T Phase 1 [123]
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 Compound Name MVT-5873 Phase 1 [15]
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 Compound Name CART-meso cells Phase 1 [124]
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 Compound Name CAR-20/19-T Cells Phase 1 [125]
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 Compound Name CARTmeso/19 Phase 1 [126]
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 Compound Name CAR-T Cells targeting Mesothelin Phase 1 [117]
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 Compound Name CAR-T Cells targeting CEA Phase 1 [117]
External Link
 Compound Name HLA-A*2402-restricted KIF20A and VEGFR-1 epitope peptide vaccine Phase 1 [127]
Synonyms
HLA-A*2402-restricted KIF20A and VEGFR-1 epitope peptide vaccine (pancreatic cancer, subcutaneous)
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External Link
 Compound Name Anti-hCD70 CAR transduced PBL Phase 1 [128]
External Link
 Compound Name MORAb-066 Phase 1 [129]
Synonyms
Anti-tissue factor monoclonal antibody (pancreatic tumor), Morphotek
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External Link
 Compound Name Anti-MUC1 mab Phase 1 [130]
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 Compound Name Anti-meso-CAR vector transduced T cells Phase 1 [131]
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 Compound Name CRS-207 + GVAX Phase 2 [51]
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 Compound Name Autologous T cells transfected with chimeric anti-mesothelin immunoreceptor SS1 Phase 1 [132]
External Link
 Compound Name Meso-CART Phase 1 [133]
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 Compound Name ASG-5ME Phase 1 [134]
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 Compound Name Anti-CD133-CAR vector-transduced T cells Phase 1 [135]
External Link
 Compound Name IRX4204 Phase 1 [18]
Synonyms
220619-73-8; CHEMBL75133; UNII-877M97Z38Y; VTP-194204; 877M97Z38Y; KB-145960; SCHEMBL3437269; MolPort-042-665-869; ZINC1550770; IRX-4204; 3-Methyl-5-[2-methyl-2-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-naphthalen-2-yl)-cyclopropyl]-penta-2,4-dienoic acid; BDBM50101445; DB11806; VTP 194204; (+)-VTP-194204; AGN 4204; (2E,4E)-3-Methyl-5-[(1S,2S)-2-methyl-2-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-naphthalen-2-yl)-cyclopropyl]-penta-2,4-dienoic acid
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 Compound Name AbGn-107 Phase 1 [18]
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 Compound Name LMB-100 Phase 1/2 [18]
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 Compound Name PLX7486 Phase 1 [136]
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 Compound Name CAR-T Cells targeting HER2 Phase 1 [117]
External Link
 Compound Name CAR-T Cells targeting MUCI Phase 1 [117]
External Link
 Compound Name SEL-403 Phase 1 [18]
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 Compound Name CAR-T Cells targeting PSCA Phase 1 [117]
External Link
 Compound Name Anti-CEA CAR-T cells Phase 1 [137]
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 Compound Name MVT-1075 Phase 1 [18]
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 Compound Name CAR-CLD18 T cell Clinical trial [138]
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 Compound Name CART-meso cells Clinical trial [139]
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 Compound Name PMID28460551-Compound-1 Patented [140]
External Link
 Compound Name Tanomastat Discontinued in Phase 3 [141]
Synonyms
Tanomastat (USAN/INN); (2S)-4-[4-(4-chlorophenyl)phenyl]-4-oxo-2-(phenylsulfanylmethyl)butanoic acid
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External Link
 Compound Name Larotaxel Discontinued in Phase 3 [142]
Synonyms
Benzenepropanoic acid; PNU 100940; XRP 9881; XRP9881
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External Link
 Compound Name Apricoxib Discontinued in Phase 2 [143]
Synonyms
TG01
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External Link
 Compound Name Lintitript Discontinued in Phase 2 [144]
Synonyms
SR 27897; SR 27897B; SR27897; SR-27897; SR-27897B; 1-((2-(4-(2-Chlorophenyl)thiazol-2-yl)aminocarbonyl)indolyl)acetic acid; 2-((4-(o-Chlorophenyl)-2-thiazolyl)carbamoyl)indole-1-acetic acid; 2-[2-[[4-(2-chlorophenyl)-1,3-thiazol-2-yl]carbamoyl]indol-1-yl]acetic acid
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External Link
 Compound Name Merbarone Discontinued in Phase 2 [145]
Synonyms
NSC-336628
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External Link
 Compound Name LY293111 Discontinued in Phase 2 [146]
Synonyms
Etalocib; 161172-51-6; UNII-THY6RIW44R; LY 293111; THY6RIW44R; CHEMBL329123; LY-193111; 2-[3-[3-[2-ethyl-4-(4-fluorophenyl)-5-hydroxyphenoxy]propoxy]-2-propylphenoxy]benzoic acid; VML295; Etalocib [USAN:INN]; Etalocib (USAN); GTPL2948; SCHEMBL1649516; CTK8E7596; C33H33FO6; VML 295; DTXSID70167073; YFIZRWPXUYFCSN-UHFFFAOYSA-N; MolPort-009-019-411; ZINC3930629; AC1L4328; PDSP2_001221; BDBM50029450; PDSP1_001237; 1758AH; DB12850; RT-013626; D04074; L001468; J-009797; Benzoic acid, 2-(3-(3-((5-ethyl-4'-fluoro-2-hydroxy(1,1'-bipheny
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External Link
 Compound Name HMN-214 Discontinued in Phase 1 [147]
Synonyms
N-(4-methoxyphenyl)sulfonyl-N-[2-[(E)-2-(1-oxidopyridin-4-yl)ethenyl]phenyl]acetamide; (E)-4-(2-(2-(N-Acetyl-N-((p-methoxyphenyl)sulfonyl)amino)phenyl)ethenyl)pyridine 1-oxide
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External Link
 Compound Name RG7600 Discontinued in Phase 1 [148]
External Link
 Compound Name IC261 Preclinical [149]
Synonyms
IC-261; IC 261
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External Link
 Compound Name ANAVEX 1007 Preclinical [150]
External Link
 Compound Name IPH-4201 Terminated [151]
Synonyms
MAb-16D10; MAb-J28; FAPP-targeting mAb (pancreatic cancer), Innate Pharma; FAPP-targeting mAb (pancreatic cancer), Universite de la Mediterranee/ INSERM; Feto-acinar pancreatic protein-targeting monoclonal antibodies (pancreatic cancer), Innate Pharma; Feto-acinar pancreatic protein-targeting monoclonal antibodies (pancreatic cancer), Universite de la Mediterranee/ INSERM
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External Link
 Compound Name MesoTarg Investigative [152]
External Link
 Compound Name PAT-PM-1 Investigative [152]
Synonyms
PM-1; Human monoclonal antibody (pancreatic cancer), Patrys; Human MAb (pancreas cancer), OncoMab/ Acceptys; Human monoclonal antibody (pancreatic cancer), OncoMab/ Acceptys; PM-1 antibody, OncoMab/ Acceptys
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External Link
 Compound Name OP-04 Investigative [152]
Synonyms
OP-04 program (prodrug, pancreatic cancer); OP-04 program (prodrug, pancreatic cancer), Onco-Pharmakon
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External Link
 Compound Name VLI-27 Investigative [153]
Synonyms
AKT inhibitor (pancreatic cancer), NovaLead Pharma
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External Link
 Compound Name GS-326 Investigative [152]
Synonyms
GS-326C
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 Compound Name PX-12 Phase 2 [154]
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 Compound Name Prodigiosin Investigative [152]
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 Compound Name Pbi-shPDX-1 LP Investigative [152]
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 Compound Name Gastrin 17C diphtheria toxoid conjugate Investigative [152]
Synonyms
Gastrin 17C diphtheria toxoid conjugate (pancreatic cancer)
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 Compound Name HS-P1 Investigative [152]
Synonyms
HS-310; Endoplasmin modulator (pancreas tumor, HeatShock/fusion protein/antigen), Heat Biologics; Gp-96-Ig + unspecified tumor antigen secreting live cell vaccine (pancreas tumor, HeatShock), Heat Biologics
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References
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Ref 68 ClinicalTrials.gov (NCT04683939) Phase I/IIa, First-in-human, Open-label, Dose Escalation Trial With Expansion Cohorts to Evaluate Safety, Pharmacokinetics, Pharmacodynamics, and Preliminary Efficacy of BNT141 as a Monotherapy and in Combination With Other Anti-cancer Agents in Patients With CLDN18.2-positive Solid Tumors. U.S.National Institutes of Health.
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Ref 84 ClinicalTrials.gov (NCT01020006) Study of Safety and Tolerability of PCI-27483 in Patients With Pancreatic Cancer Patients Receiving Treatment With Gemcitabine. U.S. National Institutes of Health.
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Ref 86 ClinicalTrials.gov (NCT02640209) Pilot Trial Of Autologous T Cells Engineered To Express Anti-CD19 Chimeric Antigen Receptor (CART19)In Combination With Ibrutinib In Patients With Relapsed Or Refractory CD19+ Chronic Lymphocytic Leukemia (CLL)Or Small Lymphocytic Lymphoma (SLL)
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Ref 98 ClinicalTrials.gov (NCT03681951) First-time-in-human (FTIH) Study of GSK3145095 Alone and in Combination With Other Anticancer Agents in Adults With Advanced Solid Tumors. U.S. National Institutes of Health.
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Ref 102 Clinical pipeline report, company report or official report of Northwest BioTherapeutics.
Ref 103 ClinicalTrials.gov (NCT02346370) A Phase 1b/2, Study of Pegylated Recombinant Human Hyaluronidase Combined With Docetaxel Versus Docetaxel Alone in Subjects With Recurrent Previously Treated Locally Advanced or Metastatic NSCLC.. U.S. National Institutes of Health.
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Ref 114 ClinicalTrials.gov (NCT04104672) A Study to Evaluate the Safety and Tolerability of AB680 in Participants With Gastrointestinal Malignancies. U.S. National Institutes of Health.
Ref 115 Clinical pipeline report, company report or official report of Statera Biopharma
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Ref 117 ClinicalTrials.gov (NCT03267173) Evaluate the Safety and Efficacy of CAR-T in the Treatment of Pancreatic Cancer.
Ref 118 ClinicalTrials.gov (NCT03323944) CAR T Cell Immunotherapy for Pancreatic Cancer
Ref 119 Clinical pipeline report, company report or official report of Otsuka Pharmaceutical Co Ltd.
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Ref 123 ClinicalTrials.gov (NCT02349724) A Clinical Research of CAR T Cells Targeting CEA Positive Cancer
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Ref 125 ClinicalTrials.gov (NCT03375619) Long-term Follow-up Study of Patients Receiving CAR-20/19-T Cells
Ref 126 ClinicalTrials.gov (NCT03497819) Autologous CARTmeso/19 Against Pancreatic Cancer
Ref 127 Phase I clinical trial of peptide vaccination with URLC10 and VEGFR1 epitope peptides in patients with advanced gastric cancer. Int J Oncol. 2014 Mar;44(3):662-8.
Ref 128 ClinicalTrials.gov (NCT02830724) Administering Peripheral Blood Lymphocytes Transduced With a CD70-Binding Chimeric Antigen Receptor to People With CD70 Expressing Cancers
Ref 129 ClinicalTrials.gov (NCT01761240) Dose Escalation Study MORAb-066 Targeting TF-expressing Malignancies Including Breast, Pancreatic, Colorectal, NSCLC. U.S. National Institutes of Health.
Ref 130 Clinical pipeline report, company report or official report of Quest PharmaTech.
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Ref 132 ClinicalTrials.gov (NCT01897415) Autologous Redirected RNA Meso CAR T Cells for Pancreatic Cancer
Ref 133 ClinicalTrials.gov (NCT02706782) A Study of Mesothelin Redirected Autologous T Cells for Advanced Pancreatic Carcinoma
Ref 134 2011 Pipeline of Seattle Genetics.
Ref 135 ClinicalTrials.gov (NCT02541370) Treatment of Relapsed and/or Chemotherapy Refractory Advanced Malignancies by CART133
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Ref 137 ClinicalTrials.gov (NCT03682744) CAR-T Intraperitoneal Infusions for CEA-Expressing Adenocarcinoma Peritoneal Metastases or Malignant Ascites (IPC)
Ref 138 ClinicalTrials.gov (NCT03302403) Clinical Study of Redirected Autologous T Cells With a Chimeric Antigen Receptor in Patients With Malignant Tumors
Ref 139 ClinicalTrials.gov (NCT03638193) Study of Autologous T-cells in Patients With Metastatic Pancreatic Cancer
Ref 140 Cancer stem cell (CSC) inhibitors: a review of recent patents (2012-2015). Expert Opin Ther Pat. 2017 Jul;27(7):753-761. doi: 10.1080/13543776.2017.1325465. Epub 2017 May 5.
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Ref 142 Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800010227)
Ref 143 Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800026002)
Ref 144 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Ligand id: 890).
Ref 145 Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800000894)
Ref 146 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Ligand id: 2948).
Ref 147 Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800010558)
Ref 148 Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800035599)
Ref 149 Circadian rhythm as a therapeutic target. Nat Rev Drug Discov. 2021 Apr;20(4):287-307.
Ref 150 2011 Pipeline of Anavex.
Ref 151 Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800017007)
Ref 152 The ChEMBL database in 2017. Nucleic Acids Res. 2017 Jan 4;45(D1):D945-D954.
Ref 153 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Target id: 1479).
Ref 154 A Randomized Phase II Study of PX-12, an Inhibitor of Thioredoxin in Patients With Advanced Cancer of the Pancreas Following Progression After a Gemcitabine-Containing Combination. Cancer Chemother Pharmacol. 2011 Mar;67(3):503-9.