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NOT YET RECRUITING
NCT07861932
PHASE1/PHASE2

A Phase 1/2a Study of K-1728 in Advanced Solid Tumors

Sponsor: KymaThera, Inc.

View on ClinicalTrials.gov

Summary

This first-in-human, open-label, multicenter study evaluates K-1728 administered as monotherapy and in combination in participants with advanced or metastatic solid tumors. The study assesses the safety, tolerability, pharmacokinetics, and preliminary antitumor activity of K-1728.

Official title: A First-in-Human Study of K-1728 Administered Alone and in Combination in Participants With Advanced or Metastatic Solid Tumors

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

110

Start Date

2026-10

Completion Date

2029-03

Last Updated

2026-10-06

Healthy Volunteers

No

Interventions

DRUG

K-1728

K-1728 will be administered orally once daily in 28-day cycles

DRUG

Fulvestrant

Fulvestrant will be administered intramuscularly on Days 1 and 15 of Cycle 1, and then Day 1 of each subsequent 28-day cycle

DRUG

Palbociclib

Palbociclib will be administered orally on Days 1-21 in 28-day cycles