Biomarker & Intervention Discovery

Ovarian Cancer

This page lists 12 druggable gene targets, 47 approved or trial-tested drug candidates and 15 recent clinical trials for Ovarian Cancer, with each agent ranked by the strength of its evidence (clinical, mechanistic or correlative). Candidates include existing drugs that could be repurposed. Sources are linked so you can check every claim.

US DALYs335.5KWHO GHE 2021 · all ages
Global DALYs5.82MWHO GHE 2021 · worldwide
US mortality13.5K deaths/yrWHO GHE 2021
Global mortality191.0K deaths/yrWHO GHE 2021 · worldwide
NIH funding$177MFY2025 · RCDC estimate
Funding levelModerate
Spontaneous remissionNo spontaneous remission; 5-year survival Stage I: 90%; Stage III/IV: 25-30%; most patients (75%) present at Stage…
Best-intervention remissionDebulking surgery + carboplatin/paclitaxel: 70-80% initial response; PARP inhibitors (olaparib, rucaparib) maintenance…
Gap sizeLarge — PARP inhibitors dramatically improve outcomes in BRCA-mutant patients; HRD testing not universal; no effective…
Primary barrieraccess + biological
Full remission profile →

Remission & chronicity

Spontaneous remission
No spontaneous remission; 5-year survival Stage I: 90%; Stage III/IV: 25-30%; most patients (75%) present at Stage III-IV
Best-intervention remission
Debulking surgery + carboplatin/paclitaxel: 70-80% initial response; PARP inhibitors (olaparib, rucaparib) maintenance in BRCA-mutant: 56% 5-year PFS vs 13.8% placebo (SOLO-1); bevacizumab maintenance: modest PFS benefit; dose-dense paclitaxel: 72.1% vs 65.1% OS at 3 years
Gap size
Large — PARP inhibitors dramatically improve outcomes in BRCA-mutant patients; HRD testing not universal; no effective screening exists
Primary barrier
access + biological
BRCA1/2 and HRD testing is not universal despite major impact on PARP inhibitor eligibility; bevacizumab access limited by cost; most patients are diagnosed at advanced stage due to no screening modality; CA-125 + transvaginal ultrasound screening trials (UKCTOCS) failed to show mortality reduction

Biomarker Targets & Therapeutic Agents

Gene targets queried against DGIdb, Open Targets, ChEMBL, PubMed, and Europe PMC. Agents ranked: Clinical > Mechanistic > Correlative.

BRCA1 283BRCA2 19CCNE1 15FOLR1 80KDR 382MSLN 9PARP1 207PARP2 189PIK3CA 444SLC34A2 71TP53 652VEGFA 207
Therapeutic Agent Effect Direction Evidence Tier Potency Source
7-HYDROXY ISOFLAVONE ? unclear Mechanistic
OLAPARIB ? unclear Mechanistic
PLATINUM COMPOUND ? unclear Mechanistic
DAIDZIN ? unclear Mechanistic
CHEMBL:CHEMBL581929 ? unclear Mechanistic
PIDNARULEX ? unclear Mechanistic
CHEMBL:CHEMBL1481721 ? unclear Mechanistic
CHEMBL:CHEMBL484663 ? unclear Mechanistic
CHEMBL:CHEMBL1214407 ? unclear Mechanistic
2-PHENYLQUINOLINE ? unclear Mechanistic
HARMALOL ? unclear Mechanistic
CHEMBL:CHEMBL1574420 ? unclear Mechanistic
DOXORUBICIN HYDROCHLORIDE ? unclear Mechanistic
MITOMYCIN ? unclear Mechanistic
PACLITAXEL PROTEIN-BOUND ? unclear Mechanistic
RESVERATROL ? unclear Mechanistic
CHEMBL:CHEMBL12658 ? unclear Mechanistic
ONONIN ? unclear Mechanistic
CEDIRANIB ? unclear Mechanistic
PIPERINE ? unclear Mechanistic
CHEMBL:CHEMBL446567 ? unclear Mechanistic
CHEMBL:CHEMBL546649 ? unclear Mechanistic
DEPHOSTATIN ? unclear Mechanistic
SEMUSTINE ? unclear Mechanistic
CISPLATIN ? unclear Mechanistic
CHEMBL:CHEMBL1404865 ? unclear Mechanistic
QUARFLOXIN ? unclear Mechanistic
PARP/TANKYRASE INHIBITOR 2X-121 ? unclear Mechanistic
WISTIN ? unclear Mechanistic
CHRYSIN DIMETHYL ETHER ? unclear Mechanistic
GEMCITABINE ? unclear Mechanistic
CHEMBL:CHEMBL600315 ? unclear Mechanistic
AURINTRICARBOXYLIC ACID ? unclear Mechanistic
MITOXANTRONE HYDROCHLORIDE ? unclear Mechanistic
SACITUZUMAB GOVITECAN ? unclear Mechanistic
CHEMBL:CHEMBL588683 ? unclear Mechanistic
CHEMBL:CHEMBL593254 ? unclear Mechanistic
CHEMBL:CHEMBL588525 ? unclear Mechanistic
PURPURIN ? unclear Mechanistic
CHEMBL:CHEMBL316796 ? unclear Mechanistic

Showing top 40 of 283 agents ranked by evidence tier.

Therapeutic Agent Effect Direction Evidence Tier Potency Source
CARBOPLATIN ? unclear Mechanistic
OLAPARIB ? unclear Mechanistic
TALAZOPARIB ? unclear Mechanistic
NIRAPARIB ? unclear Mechanistic
RUCAPARIB ? unclear Mechanistic
QUARFLOXIN ? unclear Mechanistic
CISPLATIN ? unclear Mechanistic
VELIPARIB ? unclear Mechanistic
BOSUTINIB ? unclear Mechanistic
PLATINUM COMPOUND ? unclear Mechanistic
TEMOZOLOMIDE ? unclear Mechanistic
ENZALUTAMIDE ? unclear Mechanistic
DASATINIB ANHYDROUS ? unclear Mechanistic
GEMCITABINE ? unclear Mechanistic
PIDNARULEX ? unclear Mechanistic
SACITUZUMAB GOVITECAN ? unclear Mechanistic
CEDIRANIB ? unclear Mechanistic
INIPARIB ? unclear Mechanistic
PARP/TANKYRASE INHIBITOR 2X-121 ? unclear Mechanistic
Therapeutic Agent Effect Direction Evidence Tier Potency Source
TASELISIB ? unclear Mechanistic
CAMONSERTIB ? unclear Mechanistic
FULVESTRANT ? unclear Mechanistic
ALISERTIB ? unclear Mechanistic
AMG-900 ? unclear Mechanistic
DINACICLIB ? unclear Mechanistic
LUNRESERTIB ? unclear Mechanistic
CDK INHIBITOR SNS-032 ? unclear Mechanistic
FADRACICLIB ? unclear Mechanistic
RONICICLIB ? unclear Mechanistic
PALBOCICLIB ? unclear Mechanistic
AKT INHIBITOR MK2206 ? unclear Mechanistic
AZD-5438 ↓ inhibits Mechanistic 6.0 nM (IC50)
CHEMBL5653589 ↓ inhibits Mechanistic 14.99 nM (Kd)
CHEMBL3752910 ↓ inhibits Mechanistic 74.76 nM (Kd)
Therapeutic Agent Effect Direction Evidence Tier Potency Source
MIRVETUXIMAB SORAVTANSINE ? unclear Mechanistic
VINTAFOLIDE ~ modulates Mechanistic
MIRVETUXIMAB ~ modulates Mechanistic
FARLETUZUMAB ? unclear Mechanistic
RINATABART SESUTECAN ? unclear Mechanistic
FOLATE RECEPTOR-TARGETED VINCA ALKALOID EC0489 ? unclear Mechanistic
EPOFOLATE ? unclear Mechanistic
PYRIMETHAMINE ? unclear Mechanistic
FOLIC ACID ? unclear Mechanistic
TALOTREXIN ? unclear Mechanistic
ANTIESTROGEN ? unclear Mechanistic
LOMETREXOL ? unclear Mechanistic
DEXAMETHASONE ? unclear Mechanistic
METHOTREXATE ? unclear Mechanistic 461.0 nM (IC50)
TETRAHYDROFOLIC ACID ? unclear Mechanistic
CHEMBL85871 ↓ inhibits Mechanistic 0.153 nM (Kd)
CHEMBL315627 ↓ inhibits Mechanistic 136.0 nM (Kd)
CHEMBL85848 ↓ inhibits Mechanistic 83.0 nM (Kd)
CHEMBL82390 ↓ inhibits Mechanistic 0.69 nM (Kd)
CHEMBL309415 ↓ inhibits Mechanistic 0.57 nM (Kd)
CHEMBL84935 ↓ inhibits Mechanistic 0.38 nM (Kd)
CHEMBL82261 ↓ inhibits Mechanistic 0.95 nM (Kd)
PEMETREXED ↓ inhibits Mechanistic 388.0 nM (IC50)
RALTITREXED ↓ inhibits Mechanistic 15.0 nM (IC50)
CHEMBL3335607 ↓ inhibits Mechanistic 55.7 nM (IC50)
CHEMBL3335606 ↓ inhibits Mechanistic 27.4 nM (IC50)
CHEMBL3335605 ↓ inhibits Mechanistic 9.5 nM (IC50)
CHEMBL3335604 ↓ inhibits Mechanistic 6.6 nM (IC50)
CHEMBL3335603 ↓ inhibits Mechanistic 661.0 nM (IC50)
CHEMBL1834488 ↓ inhibits Mechanistic 0.31 nM (IC50)
CHEMBL590740 ↓ inhibits Mechanistic 1.82 nM (IC50)
CHEMBL3407519 ↓ inhibits Mechanistic 550.0 nM (IC50)
CHEMBL3409334 ↓ inhibits Mechanistic 109.0 nM (IC50)
CHEMBL3409335 ↓ inhibits Mechanistic 49.3 nM (IC50)
CHEMBL3409336 ↓ inhibits Mechanistic 45.5 nM (IC50)
CHEMBL3628344 ↓ inhibits Mechanistic 0.33 nM (IC50)
CHEMBL3628345 ↓ inhibits Mechanistic 154.0 nM (IC50)
CHEMBL3628346 ↓ inhibits Mechanistic 0.61 nM (IC50)
CHEMBL3628347 ↓ inhibits Mechanistic 148.0 nM (IC50)
CHEMBL365307 ↓ inhibits Mechanistic 6.3 nM (IC50)

Showing top 40 of 80 agents ranked by evidence tier.

Therapeutic Agent Effect Direction Evidence Tier Potency Source
CEDIRANIB ↓ inhibits Mechanistic
XL820 ↓ inhibits Mechanistic
EUPATORIN ↓ inhibits Mechanistic
CABOZANTINIB S-MALATE ↓ inhibits Mechanistic
TOCERANIB ↓ inhibits Mechanistic
LAZERTINIB ↓ inhibits Mechanistic
VADIMEZAN ? unclear Mechanistic
VANDETANIB ↓ inhibits Mechanistic 70.0 nM (IC50)
SURUFATINIB ↓ inhibits Mechanistic
CANLITINIB ↓ inhibits Mechanistic
FORETINIB ↓ inhibits Mechanistic
PEGPLERANIB SODIUM ? unclear Mechanistic
REGORAFENIB ↓ inhibits Mechanistic
LINIFANIB ↓ inhibits Mechanistic
MOTESANIB ↓ inhibits Mechanistic
ILORASERTIB ↓ inhibits Mechanistic
SUNITINIB ↓ inhibits Mechanistic
COMPOUND 13A [PMID: 23639540] ↓ inhibits Mechanistic
PONATINIB ↓ inhibits Mechanistic
XL-820 ↓ inhibits Mechanistic
BX-795 ↓ inhibits Mechanistic
TELATINIB ↓ inhibits Mechanistic
SORAFENIB ↓ inhibits Mechanistic
LUCITANIB ↓ inhibits Mechanistic
PP-121 ↓ inhibits Mechanistic
NINGETINIB ↓ inhibits Mechanistic
TINENGOTINIB ↓ inhibits Mechanistic
BJ-2412 ↓ inhibits Mechanistic
VEGF RECEPTOR TYROSINE KINASE INHIBITOR III ↓ inhibits Mechanistic
PF-00337210 ↓ inhibits Mechanistic
AST-487 ↓ inhibits Mechanistic
RAMUCIRUMAB ↓ inhibits Mechanistic
AG-13958 ↓ inhibits Mechanistic
SU-14813 ↓ inhibits Mechanistic
X-82 ↓ inhibits Mechanistic
ENMD-2076 ↓ inhibits Mechanistic
GOLVATINIB ↓ inhibits Mechanistic
CENISERTIB ? unclear Mechanistic
LENVATINIB ↓ inhibits Mechanistic
SULFATINIB ↓ inhibits Mechanistic

Showing top 40 of 382 agents ranked by evidence tier.

Therapeutic Agent Effect Direction Evidence Tier Potency Source
AMATUXIMAB ? unclear Mechanistic
CRS-207 ? unclear Mechanistic
SS1(DSFV)-PE38 ? unclear Mechanistic
ANETUMAB RAVTANSINE ~ modulates Mechanistic
ANTI-MUC16/MMAE ANTIBODY-DRUG CONJUGATE DMUC4064A ? unclear Mechanistic
LMB-100 ~ modulates Mechanistic
AUTOLOGOUS MESOTHELIN-SPECIFIC CAR-T CELLS ? unclear Mechanistic
ANTI-MESOTHELIN CAR T CELLS PREPARATION ? unclear Mechanistic
RG-7600 ~ modulates Mechanistic
Therapeutic Agent Effect Direction Evidence Tier Potency Source
NIRAPARIB ↓ inhibits Mechanistic
VELIPARIB ↓ inhibits Mechanistic
4-[3-(1,4-DIAZEPAN-1-YLCARBONYL)-4-FLUOROBENZYL]PHTHALAZIN-1(2H)-ONE ↓ inhibits Mechanistic
PAMIPARIB ↓ inhibits Mechanistic
OLAPARIB ↓ inhibits Mechanistic
COMPOUND 5 [TOMASSI ET AL., 2020] ↓ inhibits Mechanistic
COMPOUND 9 [LIN ET AL., 2023] ↓ inhibits Mechanistic
INIPARIB ↓ inhibits Mechanistic
AZ1366 ↓ inhibits Mechanistic
DUAL VEGFR/PARP INHIBITOR 14B ↓ inhibits Mechanistic
NIACIN ? unclear Mechanistic
2X-121 ↓ inhibits Mechanistic
AMELPARIB DIHYDROCHLORIDE DIHYDRATE ↓ inhibits Mechanistic
CEP-9722 ? unclear Mechanistic
ORAL AZACITIDINE ? unclear Mechanistic
RUCAPARIB PHOSPHATE ↓ inhibits Mechanistic
AG14361 ↓ inhibits Mechanistic
ME0328 ↓ inhibits Mechanistic
SARUPARIB ↓ inhibits Mechanistic
SENAPARIB ↓ inhibits Mechanistic
NIRAPARIB TOSYLATE ? unclear Mechanistic
TALAZOPARIB ↓ inhibits Mechanistic
PJ34 ↓ inhibits Mechanistic
TALAZOPARIB TOSYLATE ↓ inhibits Mechanistic
PARP1 INHIBITOR (S)-G9 ↓ inhibits Mechanistic
NICARAVEN ? unclear Mechanistic
PARP-1/2 INHIBITOR ABT-767 ? unclear Mechanistic
INO-1001 ? unclear Mechanistic
BGP-15 ? unclear Mechanistic
RUCAPARIB ↓ inhibits Mechanistic
TRABECTEDIN ? unclear Mechanistic
VENADAPARIB ↓ inhibits Mechanistic
FLUZOPARIB ↓ inhibits Mechanistic
MC2050 ↓ inhibits Mechanistic
PARP INHIBITOR E7016 ? unclear Mechanistic
LERZEPARIB ↓ inhibits Mechanistic
CICLOPIROX ↓ inhibits Mechanistic
E-7016 ↓ inhibits Mechanistic
RUCAPARIB CAMSYLATE ↓ inhibits Mechanistic
PALACAPARIB ↓ inhibits Mechanistic

Showing top 40 of 207 agents ranked by evidence tier.

Therapeutic Agent Effect Direction Evidence Tier Potency Source
RUCAPARIB ↓ inhibits Mechanistic
TALAZOPARIB ↓ inhibits Mechanistic 0.85 nM (Ki)
PALACAPARIB ↓ inhibits Mechanistic
E-7016 ↓ inhibits Mechanistic
SARUPARIB ↓ inhibits Mechanistic
NIRAPARIB ↓ inhibits Mechanistic 2.1 nM (IC50)
PAMIPARIB ↓ inhibits Mechanistic 0.5 nM (IC50)
2X-121 ↓ inhibits Mechanistic
AZ1366 ↓ inhibits Mechanistic
COMPOUND 5 [TOMASSI ET AL., 2020] ↓ inhibits Mechanistic
SENAPARIB ↓ inhibits Mechanistic
TALAZOPARIB TOSYLATE ↓ inhibits Mechanistic
PARP1 INHIBITOR (S)-G9 ↓ inhibits Mechanistic
MC2050 ↓ inhibits Mechanistic
COMPOUND 10B [PMID: 26222319] ↓ inhibits Mechanistic
NIRAPARIB TOSYLATE MONOHYDRATE ↓ inhibits Mechanistic
OLAPARIB ↓ inhibits Mechanistic 1.0 nM (IC50)
RUCAPARIB CAMSYLATE ↓ inhibits Mechanistic
VELIPARIB ↓ inhibits Mechanistic 5.0 nM (Ki)
CHEMBL527654 ↓ inhibits Mechanistic 11.0 nM (Ki)
CHEMBL497608 ↓ inhibits Mechanistic 2.0 nM (Ki)
CHEMBL526668 ↓ inhibits Mechanistic 2.0 nM (Ki)
CHEMBL495743 ↓ inhibits Mechanistic 4.0 nM (Ki)
CHEMBL495942 ↓ inhibits Mechanistic 2.0 nM (Ki)
CHEMBL518484 ↓ inhibits Mechanistic 24.0 nM (Ki)
CHEMBL460267 ↓ inhibits Mechanistic 3.0 nM (Ki)
CHEMBL452801 ↓ inhibits Mechanistic 2.0 nM (Ki)
CHEMBL452800 ↓ inhibits Mechanistic 5.0 nM (Ki)
CHEMBL558845 ↓ inhibits Mechanistic 32.0 nM (IC50)
CHEMBL560790 ↓ inhibits Mechanistic 17.0 nM (IC50)
CHEMBL595018 ↓ inhibits Mechanistic 1.0 nM (IC50)
CHEMBL609002 ↓ inhibits Mechanistic 1.0 nM (IC50)
CHEMBL1089125 ↓ inhibits Mechanistic 4.0 nM (Ki)
CHEMBL1093309 ↓ inhibits Mechanistic 3.0 nM (Ki)
CHEMBL1092223 ↓ inhibits Mechanistic 23.0 nM (Ki)
CHEMBL1089474 ↓ inhibits Mechanistic 26.0 nM (Ki)
CHEMBL1093012 ↓ inhibits Mechanistic 12.0 nM (Ki)
CHEMBL1090483 ↓ inhibits Mechanistic 10.0 nM (Ki)
CHEMBL1090482 ↓ inhibits Mechanistic 18.0 nM (Ki)
CHEMBL1090136 ↓ inhibits Mechanistic 1.0 nM (Ki)

Showing top 40 of 189 agents ranked by evidence tier.

Therapeutic Agent Effect Direction Evidence Tier Potency Source
SURAMIN ? unclear Mechanistic
TEMSIROLIMUS ? unclear Mechanistic
RIGOSERTIB ↓ inhibits Mechanistic
NEOLYMPHOSTIN A ↓ inhibits Mechanistic
INAVOLISIB ↓ inhibits Mechanistic
RIGOSERTIB SODIUM ? unclear Mechanistic
TAK-733 ? unclear Mechanistic
APILIMOD DIMESYLATE CAPSULE ? unclear Mechanistic
COMPOUND 15A [PMID: 32069401] ↓ inhibits Mechanistic
COMPOUND 41 [PMID: 31855425] ↓ inhibits Mechanistic
ERDAFITINIB ? unclear Mechanistic
RIBOCICLIB ? unclear Mechanistic
BRAFV600/PI3K INHIBITOR ASN003 ? unclear Mechanistic
GSK2636771 ↓ inhibits Mechanistic
ZINC SULFATE ANHYDROUS ? unclear Mechanistic
EVEROLIMUS ? unclear Mechanistic
COPANLISIB ↓ inhibits Mechanistic
TANESPIMYCIN ? unclear Mechanistic
CAPIVASERTIB ? unclear Mechanistic
SAMOTOLISIB ↓ inhibits Mechanistic
COPANLISIB HYDROCHLORIDE ↓ inhibits Mechanistic
PAXALISIB ↓ inhibits Mechanistic
U0126 ? unclear Mechanistic
PILARALISIB ↓ inhibits Mechanistic
M-2698 ? unclear Mechanistic
GSK2334470 ? unclear Mechanistic
BIMIRALISIB ↓ inhibits Mechanistic
PALBOCICLIB ? unclear Mechanistic
SONOLISIB ↓ inhibits Mechanistic 88.0 nM (IC50)
VULOLISIB ↓ inhibits Mechanistic
ALPELISIB ↓ inhibits Mechanistic
DOCETAXEL ANHYDROUS ? unclear Mechanistic
COMPOUND 27 [PMID: 35834807] ↓ inhibits Mechanistic
MILTEFOSINE ? unclear Mechanistic
CARBOPLATIN ? unclear Mechanistic
ACALISIB ↓ inhibits Mechanistic
GEDATOLISIB ↓ inhibits Mechanistic
VS-5584 ↓ inhibits Mechanistic
XRD-0394 ↓ inhibits Mechanistic
IZORLISIB ? unclear Mechanistic

Showing top 40 of 444 agents ranked by evidence tier.

Therapeutic Agent Effect Direction Evidence Tier Potency Source
LIFASTUZUMAB VEDOTIN ~ modulates Mechanistic
COMPOUND 15 [PMID: 35034442] ↓ inhibits Mechanistic
CHEMBL4159390 ↓ inhibits Mechanistic 150.0 nM (IC50)
CHEMBL5174202 ↓ inhibits Mechanistic 120.0 nM (IC50)
CHEMBL5182987 ↓ inhibits Mechanistic 15.0 nM (IC50)
CHEMBL5171732 ↓ inhibits Mechanistic 64.0 nM (IC50)
CHEMBL5169559 ↓ inhibits Mechanistic 2881.0 nM (IC50)
CHEMBL5180542 ↓ inhibits Mechanistic 1404.0 nM (IC50)
CHEMBL5180294 ↓ inhibits Mechanistic 1140.0 nM (IC50)
CHEMBL5206581 ↓ inhibits Mechanistic 71.0 nM (IC50)
CHEMBL5188788 ↓ inhibits Mechanistic 288.0 nM (IC50)
CHEMBL5188991 ↓ inhibits Mechanistic 43.0 nM (IC50)
CHEMBL5172080 ↓ inhibits Mechanistic 103.0 nM (IC50)
CHEMBL5175794 ↓ inhibits Mechanistic 24.0 nM (IC50)
CHEMBL5173115 ↓ inhibits Mechanistic 61.0 nM (IC50)
CHEMBL5170356 ↓ inhibits Mechanistic 14.0 nM (IC50)
CHEMBL5188295 ↓ inhibits Mechanistic 257.0 nM (IC50)
CHEMBL5192917 ↓ inhibits Mechanistic 71.0 nM (IC50)
CHEMBL5205024 ↓ inhibits Mechanistic 538.0 nM (IC50)
CHEMBL5182681 ↓ inhibits Mechanistic 448.0 nM (IC50)
CHEMBL5192454 ↓ inhibits Mechanistic 369.0 nM (IC50)
CHEMBL5174538 ↓ inhibits Mechanistic 356.0 nM (IC50)
CHEMBL5175718 ↓ inhibits Mechanistic 78.0 nM (IC50)
CHEMBL5197471 ↓ inhibits Mechanistic 1015.0 nM (IC50)
CHEMBL5197826 ↓ inhibits Mechanistic 2582.0 nM (IC50)
CHEMBL5203825 ↓ inhibits Mechanistic 166.0 nM (IC50)
CHEMBL5184710 ↓ inhibits Mechanistic 535.0 nM (IC50)
CHEMBL5169500 ↓ inhibits Mechanistic 401.0 nM (IC50)
CHEMBL5206879 ↓ inhibits Mechanistic 401.0 nM (IC50)
CHEMBL5194589 ↓ inhibits Mechanistic 267.0 nM (IC50)
CHEMBL5174544 ↓ inhibits Mechanistic 1000.0 nM (IC50)
CHEMBL5185371 ↓ inhibits Mechanistic 118.0 nM (IC50)
CHEMBL5204866 ↓ inhibits Mechanistic 437.0 nM (IC50)
CHEMBL5206181 ↓ inhibits Mechanistic 713.0 nM (IC50)
CHEMBL5178362 ↓ inhibits Mechanistic 2486.0 nM (IC50)
CHEMBL5180710 ↓ inhibits Mechanistic 80.0 nM (IC50)
CHEMBL5204879 ↓ inhibits Mechanistic 36.0 nM (IC50)
CHEMBL5192822 ↓ inhibits Mechanistic 38.0 nM (IC50)
CHEMBL5185161 ↓ inhibits Mechanistic 46.0 nM (IC50)
CHEMBL5203134 ↓ inhibits Mechanistic 179.0 nM (IC50)

Showing top 40 of 71 agents ranked by evidence tier.

Therapeutic Agent Effect Direction Evidence Tier Potency Source
PIRARUBICIN ? unclear Mechanistic
OXALIPLATIN ? unclear Mechanistic
SIREMADLIN ↓ inhibits Mechanistic
CARBOPLATIN ? unclear Mechanistic
DAUNORUBICIN HYDROCHLORIDE ? unclear Mechanistic
CHEMBL:CHEMBL260560 ? unclear Mechanistic
MELPHALAN ? unclear Mechanistic
LAPACHONE ? unclear Mechanistic
VITAMIN K3 ? unclear Mechanistic
CHEMBL:CHEMBL260451 ? unclear Mechanistic
DINOSEB ? unclear Mechanistic
RIMCAZOLE ? unclear Mechanistic
TRACAZOLATE ? unclear Mechanistic
CAPIVASERTIB ? unclear Mechanistic
AZD7648 ? unclear Mechanistic
QUINALIZARIN ? unclear Mechanistic
INOSITOL ? unclear Mechanistic
ECONAZOLE NITRATE ? unclear Mechanistic
L-733,060 ? unclear Mechanistic
U50488 ? unclear Mechanistic
CHEMBL:CHEMBL260028 ? unclear Mechanistic
CHEMBL:CHEMBL601140 ? unclear Mechanistic
CHEMBL:CHEMBL408563 ? unclear Mechanistic
ENALAPRIL MALEATE ? unclear Mechanistic
HOMIDIUM BROMIDE ? unclear Mechanistic
IOXYNIL ? unclear Mechanistic
ACALABRUTINIB ? unclear Mechanistic
INDOPROFEN ? unclear Mechanistic
MERCAPTOPURINE ? unclear Mechanistic
AUTOLOGOUS DENDRITIC CELLS TRANSDUCED WITH WILD-TYPE P53 ADENOVIRUS VACCINE ? unclear Mechanistic
ZIRAM ? unclear Mechanistic
IFOSFAMIDE ? unclear Mechanistic
DOCETAXEL ANHYDROUS ? unclear Mechanistic
SOTULETINIB ? unclear Mechanistic
SERTRALINE HYDROCHLORIDE ? unclear Mechanistic
PD166285 ? unclear Mechanistic
SAPANISERTIB ? unclear Mechanistic
ENZALUTAMIDE ? unclear Mechanistic
PYRITHIONE ZINC ? unclear Mechanistic
CHEMBL:CHEMBL1169388 ? unclear Mechanistic

Showing top 40 of 652 agents ranked by evidence tier.

Therapeutic Agent Effect Direction Evidence Tier Potency Source
BEVASIRANIB ? unclear Mechanistic
RANIBIZUMAB ↓ inhibits Mechanistic
CP-547632 ? unclear Mechanistic
EW-A-401 ? unclear Mechanistic
BEVACIZUMAB 111IN ~ modulates Mechanistic
FENOFIBRATE MICRONIZED ? unclear Mechanistic
PEGAPTANIB ↓ inhibits Mechanistic
DEXAMETHASONE ? unclear Mechanistic
SQUALAMINE ? unclear Mechanistic
AFLIBERCEPT ↓ inhibits Mechanistic
PAZOPANIB ? unclear Mechanistic
BEVACIZUMAB GAMMA ~ modulates Mechanistic
CILOSTAZOL ? unclear Mechanistic
ADALIMUMAB ? unclear Mechanistic
MUPARFOSTAT ↓ inhibits Mechanistic
SILDENAFIL ? unclear Mechanistic
PENTOSAN POLYSULFATE ? unclear Mechanistic
THALIDOMIDE ? unclear Mechanistic
RISUTEGANIB ? unclear Mechanistic
SELECTIVE CYTOKINE INHIBITORY DRUG CC-1088 ? unclear Mechanistic
PHENETHYL ISOTHIOCYANATE ? unclear Mechanistic
EMVODODSTAT ? unclear Mechanistic
CARFILZOMIB ? unclear Mechanistic
FARICIMAB ↓ inhibits Mechanistic
ALBUTEROL SULFATE ? unclear Mechanistic
LENALIDOMIDE ↓ inhibits Mechanistic
SUNITINIB ? unclear Mechanistic
SHARK CARTILAGE EXTRACT AE-941 ? unclear Mechanistic
NM-3 ? unclear Mechanistic
DILPACIMAB ? unclear Mechanistic
PEMETREXED DISODIUM ? unclear Mechanistic
BI-836880 ? unclear Mechanistic
BROLUCIZUMAB ↓ inhibits Mechanistic
DOMATINOSTAT ? unclear Mechanistic
ANTHRACYCLINE ANTINEOPLASTIC ANTIBIOTIC ? unclear Mechanistic
VEGF/HGF-TARGETING DARPIN MP0250 ? unclear Mechanistic
WARFARIN ? unclear Mechanistic
CELECOXIB ? unclear Mechanistic
NAVICIXIZUMAB ? unclear Mechanistic
VEGLIN ? unclear Mechanistic

Showing top 40 of 207 agents ranked by evidence tier.


Clinical Trials

Drug, biologic and supplement trials (treatment or prevention) from ClinicalTrials.gov whose main condition is Ovarian Cancer: recruiting, active or completed, most recently updated first. Data retrieved 2026-10-28.

NCT06542549 Phase: 3 Started: 2025-03-11

This is a randomized, controlled, multicenter clinical study to evaluate AK104 in FIGO 2018 stage III-IV ovarian cancer subjects who were assessed to be at high perioperative risk and/or unable to achieve R0 resection prior to initial treatment. The efficacy and safety of neoadjuvant therapy with in...

NCT06819007 Phase: 3 Started: 2025-03-19

This clinical trial is designed to evaluate the efficacy and safety of T-DXd in combination with bevacizumab versus bevacizumab monotherapy as first-line maintenance therapy, in participants with human epidermal growth factor 2 (HER2)-expressing (immunohistochemistry \[IHC\] 3+/2+/1+) advanced high-...

NCT03363867 Phase: 2 Started: 2018-07-10

Epithelial ovarian cancer (EOC) is the ninth most common cause of cancer in Australian women, with an estimated 1500 new diagnoses in Australia in 2015, and remains the seventh most common cause of cancer death in Australian women. High grade serous ovarian cancer (HGSC) is the most common form of E...

NCT06394804 Phase: 2 Started: 2024-04-29

The researchers are doing this study to find out whether the combination of avutometinib, defactinib, and letrozole is an effective treatment for people with low-grade serous ovarian cancer (LGSOC). The researchers will also look at the safety of this combination.

NCT05460000 Phase: 2 Started: 2024-10-11

Multicenter, randomized, open label study including patients with advanced HRDpositive high-grade ovarian cancer, fallopian tube cancer, primary peritoneal cancer and clear cell carcinoma of the ovary with no residual tumor mass following primary tumor debulking to determine recurrence free survival...

NCT07489287 Phase: 1 Started: 2026-08-18

This phase 1 study evaluates the safety, efficacy, and biological activity of GB-5267 in patients with platinum-resistant ovarian cancer.

NCT07778498 Phase: 1/2 Started: 2026-09-29

The goal of this clinical trial is to evaluate whether TJ102, an investigational antibody-drug conjugate (ADC), can safely and effectively treat patients with advanced ovarian or other solid tumors. The main objectives of this study are : • To Determine the maximum tolerated dose (MTD) and recommend...

NCT07776691 Phase: 3 Started: 2026-09-18

Researchers are looking for new ways to treat ovarian cancer (OC). Current treatment for OC may start with surgery to remove as much of the cancer as possible. After surgery, people may receive chemotherapy. After chemotherapy, standard care options may include: Maintenance treatment, which is used ...

NCT06843447 Phase: 1/2 Started: 2025-04-15

Researchers are looking for other ways to treat high-grade serous and certain other ovarian cancer. High-grade means the cancer cells grow and spread quickly. Serous means the cancer started in the cells that cover the ovaries, the lining of the belly, or in the fallopian tubes. Standard treatment (...

NCT06890338 Phase: 2 Started: 2025-11-21

Cancer is a condition where cells in a specific part of body grow and reproduce uncontrollably. The purpose of this study is to assess the safety and efficacy of neoadjuvant carboplatin and mirvetuximab soravtansine in participants with folate receptor alpha (FRα) -expressing advanced-stage serous e...

NCT04374630 Phase: 2 Started: 2020-07-07

Afuresertib is an AKT inhibitor, a new class of agents under development that may provide physicians with a new clinical option to control platinum resistant ovarian cancer (PROC) progression. Afuresertib plus chemotherapy has demonstrated anti-tumor efficacy and an acceptable safety profile in pati...

NCT03854110 Phase: 1 Started: 2019-01-14

This is a phase 1 dose escalation trial of monotherapy misetionamide (also known as GP-2250) currently enrolling patients with platinum-resistant ovarian cancer (PROC) into Part 2 of the study. Part 1 of the study evaluating misetionamide in combination with gemcitabine in subjects with advanced pan...

NCT07743164 Phase: 3 Started: 2026-10-07

Researchers are looking for new ways to treat advanced, high-grade ovarian cancer (OC). Advanced means the cancer has spread to other parts of the body (metastatic) and may not be removed with surgery. High-grade means the cancer cells grow and spread quickly. This trial includes types of OC that st...

NCT07665515 Phase: 1 Started: 2026-09

Ovarian, fallopian tube, or primary peritoneal cancer, collectively referred to as ovarian cancer, remains the deadliest type of gynaecological cancer. The most common and aggressive form is called high-grade serous ovarian cancer. The main purpose of this study is to understand whether an experimen...

NCT07816666 Phase: 3 Started: 2026-09-24

The purpose of this study is to measure the efficacy and safety of torvutatug samrotecan (torvu-sam) with or without bevacizumab compared to standard of care (SoC) as maintenance treatment in participants with platinum-sensitive relapsed ovarian cancer (PSR OC)


Agents Found By Disease-Level Search

Searched directly from “Ovarian Cancer” via ClinicalTrials.gov interventions and Open Targets' disease→drug data — independent of the 12-gene target panel above. This surfaces agents whose mechanism doesn't route through a curated gene (combination therapies, standard-of-care drugs, targets outside the panel).

47 agents shown (approved or with trial evidence) — 39 not found by the gene-target search above.

Carboplatin

Approved · 7 trials · source: ClinicalTrials.gov, Open Targets
NCT00214058 NCT00189553 NCT00989651

PaclitaxelNOT in gene-target list

Phase 3 · 7 trials · source: ClinicalTrials.gov, Open Targets
NCT00189553 NCT00989651 NCT06023862

Bevacizumab

Pre-approval · 5 trials · source: ClinicalTrials.gov, Open Targets
NCT06307249 NCT01091259 NCT00989651

Olaparib

Approved · 4 trials · source: ClinicalTrials.gov, Open Targets
NCT05887609 NCT04532645 NCT03579316

Gemcitabine

Phase 3 · 3 trials · source: ClinicalTrials.gov, Open Targets
NCT04616534 NCT06023862 NCT07604766

Metformin

Phase 2 · 3 trials · source: ClinicalTrials.gov, Open Targets
NCT03792984 NCT00159536 NCT06015594

Cisplatin

Phase 3 · 3 trials · source: ClinicalTrials.gov, Open Targets
NCT00989651 NCT00003896 NCT00006036

filgrastimNOT in gene-target list

Phase 3 · 3 trials · source: ClinicalTrials.gov, Open Targets
NCT00004066 NCT00002977 NCT00467051

DocetaxelNOT in gene-target list

Phase 2 · 2 trials · source: ClinicalTrials.gov, Open Targets
NCT00214058 NCT00004066

Letrozole

Phase 2/3 · 2 trials · source: ClinicalTrials.gov, Open Targets
NCT06418347 NCT02389088

2X-121

Phase 2 · 2 trials · source: ClinicalTrials.gov, Open Targets
NCT03878849 NCT03878849

Pegylated liposomal doxorubicinNOT in gene-target list

· 2 trials · source: ClinicalTrials.gov
NCT00189553 NCT06023862

ChemotherapyNOT in gene-target list

· 2 trials · source: ClinicalTrials.gov
NCT02728622 NCT07033819

ZoladexNOT in gene-target list

· 1 trial · source: ClinicalTrials.gov
NCT01712893

quadratus lumborum blockNOT in gene-target list

· 1 trial · source: ClinicalTrials.gov
NCT06397300

lumbar epiduralNOT in gene-target list

· 1 trial · source: ClinicalTrials.gov
NCT06397300

Neoantigen polypeptide vaccineNOT in gene-target list

· 1 trial · source: ClinicalTrials.gov
NCT06341907

ElimusertibNOT in gene-target list

Phase 1 · 1 trial · source: ClinicalTrials.gov, Open Targets
NCT04616534

Bipolar coagulation forceps (ETHICON inc.)NOT in gene-target list

· 1 trial · source: ClinicalTrials.gov
NCT03109964

SURGIFLO hemostatic matrix (ETHICON inc.)NOT in gene-target list

· 1 trial · source: ClinicalTrials.gov
NCT03109964

Alpha lipoic acidNOT in gene-target list

· 1 trial · source: ClinicalTrials.gov
NCT06418347

SNPNOT in gene-target list

· 1 trial · source: ClinicalTrials.gov
NCT06307249

Palbociclib 125mgNOT in gene-target list

· 1 trial · source: ClinicalTrials.gov
NCT06307249

Vitamin B ComplexNOT in gene-target list

· 1 trial · source: ClinicalTrials.gov
NCT07191587

mirvetuximab soravtansine (MIRV; IMGN853)NOT in gene-target list

· 1 trial · source: ClinicalTrials.gov
NCT04606914

Vitamin D3NOT in gene-target list

· 1 trial · source: ClinicalTrials.gov
NCT03792984

Calcium CarbonateNOT in gene-target list

· 1 trial · source: ClinicalTrials.gov
NCT03792984

Cinnamon Cap 500 MGNOT in gene-target list

· 1 trial · source: ClinicalTrials.gov
NCT03778099

DoxilNOT in gene-target list

· 1 trial · source: ClinicalTrials.gov
NCT00945139

AvastinNOT in gene-target list

· 1 trial · source: ClinicalTrials.gov
NCT00945139

Indication-extended Fertility-sparing TherapyNOT in gene-target list

· 1 trial · source: ClinicalTrials.gov
NCT05945407

therapeutic autologous lymphocytesNOT in gene-target list

· 1 trial · source: ClinicalTrials.gov
NCT00101257

Anthropometric and physical examinationNOT in gene-target list

· 1 trial · source: ClinicalTrials.gov
NCT03841981

Indirect calorimetry, accelerometer and seven-day dietary recallNOT in gene-target list

· 1 trial · source: ClinicalTrials.gov
NCT03841981

Biochemical, hormonal and metabolic phenotypingNOT in gene-target list

· 1 trial · source: ClinicalTrials.gov
NCT03841981

Sonographic studiesNOT in gene-target list

· 1 trial · source: ClinicalTrials.gov
NCT03841981

Cardiovascular autonomic function studiesNOT in gene-target list

· 1 trial · source: ClinicalTrials.gov
NCT03841981

Oral smear and feces specimenNOT in gene-target list

· 1 trial · source: ClinicalTrials.gov
NCT03841981

ECoFamNOT in gene-target list

· 1 trial · source: ClinicalTrials.gov
NCT07129434

Escitalopram 20 mgNOT in gene-target list

· 1 trial · source: ClinicalTrials.gov
NCT05840692

CM-24 and Nivolumab - Dose EscalationNOT in gene-target list

· 1 trial · source: ClinicalTrials.gov
NCT04731467

CM-24, Nivolumab, Nab paclitaxel and Gemcitabine - ExpansionNOT in gene-target list

· 1 trial · source: ClinicalTrials.gov
NCT04731467

CM-24, Nivolumab, and Nal-IRI/5-FU/LV - ExpansionNOT in gene-target list

· 1 trial · source: ClinicalTrials.gov
NCT04731467

Nivolumab, Nab paclitaxel and Gemcitabine - ExpansionNOT in gene-target list

· 1 trial · source: ClinicalTrials.gov
NCT04731467

Nivolumab and Nal-IRI/5-FU/LV - ExpansionNOT in gene-target list

· 1 trial · source: ClinicalTrials.gov
NCT04731467

veliparib (ABT-888)NOT in gene-target list

· 1 trial · source: ClinicalTrials.gov
NCT02210663

ETX-19477NOT in gene-target list

· 1 trial · source: ClinicalTrials.gov
NCT06395519

Generated by the Open Source Medicine Foundation Biomarker Pipeline — 2026-10-08. Data sources: DGIdb, Open Targets, ChEMBL, PubMed, ClinicalTrials.gov. Not medical advice.