VT3989 enables a pipeline of clinical trials within a single product.

Our clinical development plan represents a staged strategy to maximize the benefit for increasingly broader groups of patients.

  1. Initiate the Phase 3 sTEADfast study in 2nd and 3rd line Mesothelioma patients previously treated with both immunotherapy and chemotherapy.
  2. Prolong progression-free survival by combining VT3989 with standard of care immunotherapy and chemotherapy regimens in first line Mesothelioma patients in Phase 2 expansion cohorts.
  3. Demonstrate proof of concept of VT3989 synergy and resistance prevention to other targeted agents such as EGFR inhibitors, KRAS G12C inhibitors and panRAS(on) inhibitors.

Indication

Preclinical

Phase 1

P1

P2

P3

Phase 2

Phase 3

2L/3L Mesothelioma

VT3989 monotherapy

FPI planned
Dec 2026

1L Mesothelioma

VT3989 + ipilimumab + nivolumab

Actively enrolling

VT3989 + platinum + pemetrexed

Actively enrolling

EGFRm NSCLC

KRAS G12C CRC**

Pancreatic**

VT3989 + osimertinib

Actively enrolling

VT3989 + KRASG12Ci
VT3989 + KRASG12Ci

EHE* and Meningioma

VT3989 monotherapy

* EHE: epithelioid hemangioendothelioma
** Planned investigator sponsored trials

Actively Enrolling

Details about Vivace’s ongoing Phase I/II clinical trial of VT3989 can be found at https://clinicaltrials.gov

Combination Study Opportunities

Companies with mechanisms that synergize with TEAD inhibitors and would like to explore a collaboration should contact Vivace at info@vivacetherapeutics.com

Investigator Sponsored Trials

Investigators interested in exploring partnerships to study VT3989 in their clinic should contact Vivace at info@vivacetherapeutics.com  

Phase 3 sTEADfast study of VT3989 monotherapy vs standard of care salvage chemotherapy with gemcitabine or vinorelbine in Mesothelioma patients previously treated with both immunotherapy and chemotherapy is set to begin enrolling shortly

For more information on the Phase 3 sTEADfast trial contact Vivace at info@vivacetherapeutics.com