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Recently added Catalysts

vopimetostat

Phase 1

PDAC | Small molecule | Oncology |Erasca, Inc.|Trials Updated: Oct 27, 2026

vopimetostat development status

Highest phase Phase 1
Registered trials 1 across 1 sponsor since Oct 2026

Success Probability

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Market & Valuation

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Trial Design

CONTROLLEDBiomarker
Total Trials1
Total Enrollment188

FDA Designations

No designations recorded

vopimetostat clinical trials

vopimetostat · 1 trial · 8 indications

Phase 1 1
NCT07897734TNG462-C103: Study to Evaluate the Safety, Tolerability, and Antitumor Activity of Vopimetostat in Combination With ERAS-0015 in PDAC and NSCLC PatientsPDAC
NOT YET_RECRUITING188 Analytics
PHASE1NOT YET_RECRUITING
TNG462-C103: Study to Evaluate the Safety, Tolerability, and Antitumor Activity of Vopimetostat in Combination With ERAS-0015 in PDAC and NSCLC Patients
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Study Endpoints

Primary Endpoints

Phase 1 Maximum Tolerated Dose
21 days

To determine the MTD and RD(s) of vopimetostat in combination with ERAS-0015

Phase 2 Combination Anti-neoplastic Activity
12 weeks

To assess antitumor activity- ORR of vopimetostat in combination with ERAS-0015

Secondary Endpoints

Phase 1 and 2 Combination Anti-neoplastic Activity
12 weeks
Phase 1 and 2 PK Profile of vopimetostat and ERAS-0015 in Combination
21 days
Phase 1 and 2 Adverse Event Profile
21 days
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Study Design & Arms

AllocationNON_RANDOMIZED
MaskingNONE
ModelSEQUENTIAL
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
Dose Escalation PDACEXPERIMENTALEscalating doses of vopimetostat in combination with ERAS-0015
Dose expansion 1L PDACEXPERIMENTALExpansion arm at the RD(s) of vopimetostat in combination with ERAS-0015
Dose Expansion 2L PDACEXPERIMENTALExpansion arm at the RD(s) of vopimetostat in combination with ERAS-0015
Dose Expansion 2L or 3L NSCLCEXPERIMENTALExpansion arm at the RD(s) of vopimetostat in combination with ERAS-0015

Interventions

NameTypeDescription
vopimetostatDRUGMTA-cooperative PRMT5 inhibitor
ERAS-0015DRUGPan-RAS molecular glue
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Eligibility Criteria

Age Range18 Years to N/A
SexALL
Healthy VolunteersNo

Inclusion Criteria: 1. Is ≥18 years of age at the time of signature of the main study ICF. 2. Has an ECOG PS of 0 or 1. 3. Has loss of the MTAP gene, documented by a validated assay 4. Has one of the following disease characteristics: * 1L or 2L metastatic PDAC * Locally advanced, recurrent ...

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Recent Changes (Last 90 Days)

LOWOct 27, 2026NCT07897734NEW_TRIAL: changed
LOWOct 27, 2026NCT07897734NEW_TRIAL: changed