Clinical trials

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Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

A Study to Evaluate the Safety, Pharmacokinetics, and Anti-Tumor Activity of VVD-133214 as Monotherapy and in Combination in Participants With Advanced Solid Tumors

This is a first-in-human, Phase I, open-label, multicenter, dose-escalation and dose expansion study to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and preliminary anti-tumor activity of VVD-133214 monotherapy, and in combination with bevacizumab or pembrolizumab, in participants with microsatellite instability (MSI) and/or deficient mismatch repair (dMMR) advanced solid tumors. VVD-133214 is an oral drug that acts on a protein called Werner (WRN), which may promote the growth of cancers that are MSI and/or dMMR. By acting on WRN, VVD-133214 may be able to block the growth of these types of cancer.

Participants needed: 280
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: Vividion Therapeutics, Inc.Updated: Aug 17, 2026Locations: 43
Eligibility criteria

Eastern Cooperative Oncology Group (ECOG) performance status score of 0 or 1 [+6]

Inability or unwillingness to swallow pills [+21]

Status: Recruiting

A First-in-Human (FIH) Study to Evaluate the Safety and Tolerability of VVD-130037 in Participants With Advanced Solid Tumors

A FIH dose escalation and dose expansion study to evaluate VVD-130037 in participants with advanced solid tumors as a single agent, and in combination with docetaxel, paclitaxel, or pembrolizumab.

Participants needed: 290
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: Vividion Therapeutics, Inc.Updated: May 8, 2026Locations: 26
Eligibility criteria

Histologically or cytologically confirmed metastatic or unresectable solid tumor... [+10]

KEAP1 nonsense mutation (any position) [+9]

Status: Recruiting

A First-in-Human (FIH) Study to Evaluate the Safety and Tolerability of VVD-159642 in Participants With Advanced Solid Tumors

A FIH study to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and preliminary anti-tumor activity of VVD-159642, a rat sarcoma viral oncogene-phosphatidylinositol 3-kinase alpha (RAS-PI3Kα) inhibitor, as a single agent and in combination with either sotorasib or trametinib in participants with advanced solid tumors.

Participants needed: 220
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: Vividion Therapeutics, Inc.Updated: Mar 18, 2026Locations: 9
Eligibility criteria

For Part 1 Dose Escalation, the prospective participant must have histologically... [+5]

Active central nervous system (CNS) malignancies. [+5]