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Study details
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PTX-912 Clinical Trial

Proviva Therapeutics, Inc.
NCT IDNCT06190886ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1

Target enrollment

26

Study length

about 2.1 years

Ages

18+

Locations

3 sites in CA, FL, NE

About this study

This trial is testing the safety and how well PTX-912 works in people with advanced or metastatic solid tumors. The goal is to determine a safe dose of PTX-912, understand its effects on the body (pharmacokinetics), and see if it has any anti-cancer activity.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take PTX-912
PhasePhase 1
Primary goalDLTs (dose limiting toxicity)

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low15%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

Endpoints

Primary: DLTs (dose limiting toxicity)

Body systems

Oncology