Last reviewed · How we verify

NCT06779851: SUMMIT-1

A Study to Evaluate Safety and Tolerability of BPT567 in Patients With Advanced Solid Tumors

Active, enrolled Phase 1 Last updated 13 February 2026
What this trial tests

Phase 1 trial testing BPT567 in Advanced Solid Tumors in 100 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
15 October 2024
Primary endpoint
31 December 2027
31 December 2028

Quick facts

Lead sponsorBright Peak Therapeutics Inc
PhasePhase 1
StatusActive, enrolled
Study typeINTERVENTIONAL
Allocationnon randomized
Designsequential
Maskingnone
Primary purposetreatment
Enrollment100
Start date15 October 2024
Primary completion31 December 2027
Estimated completion31 December 2028
Sites7 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Bright Peak Therapeutics Inc — full company profile →

Who can join

18 and older, any sex, with Advanced Solid Tumors. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a first-in-human Phase Ia/Ib, open-label, multicenter, dose escalation and dose expansion study designed to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and maximum tolerated dose (MTD) or maximum adminstered dose (MAD) of BPT567 in patients with advanced solid tumors, and establish the recommended dose for expansion cohorts.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other recruiting trials for Advanced Solid Tumors

Currently open trials in the same condition.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06779851.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing