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RecruitingLast updated: 17 April 2026

C4901001: A study evaluating a drug called PF-07799544 in people with advanced solid cancers with a BRAF V600 mutationA PHASE 1A/B OPEN-LABEL MASTER STUDY OF PF-07799544 AS A SINGLE-AGENT AND IN COMBINATION WITH OTHER TARGETED AGENTS IN PARTICIPANTS WITH ADVANCED SOLID TUMORS

Trial purpose

Medical clipboardCancer treatment

Tumor type

Multi-Cancer Multi-Cancer

Age

People16+

Trial acronym

C4901001

Clinical summary

Summary

The purpose of this clinical trial is to learn the safety and effects of a new drug (called PF-07799544) when administered alone and in combination with other medication in people with solid cancers. 

The study has two parts. In Phase 1a where PF-07799544 was given by itself. Phase 1a is not longer open to recruitment.

In Phase 1b, PF-07799544 will be given with another study medicine (called PF-07799933).

In Phase 1b (described below), researchers are seeking participants who have:

  • a solid tumour which is metastatic or recurrent (excluding colorectal cancer)
  • tumour with a mutation n(abnormal gene) called "BRAF V600"
  • received required prior treatment for cancer per cohort assigned.

All participants in this study will receive both study medicines. Both study medicines are tablets that are taken by mouth at home twice a day.

Participants will receive study medicines until their cancer is no longer responding, unacceptable side effects, or 2 years. Participants may continue to receive study therapy beyond 2 years. We will examine the experiences of people receiving the study medicines. This will help us determine if the study medicines are safe and effective.

 

Conditions

This trial is treating people with advanced or metastatic solid cancer (excluding colorectal cancer) with evidence of BRAF V600 mutation

Eligibility

Inclusion

Phase 1b Inclusion Criteria:

  • Diagnosis of advanced/metastatic solid tumor (excluding colorectal cancer)
  • Measurable disease by RECIST version 1.1
  • Evidence of a BRAF V600 mutation
  • Prior therapy per tumor cohort
  • Adequate organ function per protocol

Exclusion

Phase 1b Exclusion Criteria:

  • Other active malignancy within 3 years
  • Presence of leptomeningeal disease
  • History or current evidence of retinal vein occlusion (RVO) or history of retinal degenerative disease
  • Concurrent neuromuscular disorder associated with elevated creatine kinase (CK)
  • Active gastrointestinal disease as defined per protocol
  • History of interstitial lung disease as defined per protocol

Inclusion

  • You have had treatment, but your cancer has come back (relapsed or recurrent).
  • Your cancer has spread to other parts of the body (metastatic) or has grown into nearby parts of the body (locally advanced).
  • Your cancer has not spread to other parts of the body, but it is not possible to perform surgery to remove it (unresectable).
  • You have had treatment but your cancer has gotten worse or has not responded to the treatment you have been given.
  • You are able to swallow medication by mouth.

Exclusion

  • You have been diagnosed with a prior or secondary type of cancer.
  • You have certain types of non-cancer medical conditions.
Message

Clinical trials have complex eligibility criteria, and other criteria may apply for this trial. Ask your doctor about whether this trial could be right for you.

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More information

Trial Identifiers

Information on this page is partially produced from ClinicalTrials.gov *. View further details about this trial on the registry via the links below:

Trial sponsor

Pfizer

Scientific Title

A PHASE 1A/B OPEN-LABEL MASTER STUDY OF PF-07799544 AS A SINGLE-AGENT AND IN COMBINATION WITH OTHER TARGETED AGENTS IN PARTICIPANTS WITH ADVANCED SOLID TUMORS

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