Study of PF-07265807 in Participants With Metastatic Solid Tumors.
NCT04458259 · Status: TERMINATED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 88
Last updated 2025-08-28
Summary
A First-in-Human Pharmacokinetic, Safety, and Tolerability Study of PF-07265807 as Monotherapy and in Combination in Participants with Advanced or Metastatic Solid Tumors
Conditions
- Neoplasm Metastasis
Interventions
- DRUG
-
PF-07265807
Given 2 weeks on/1 week off
- DRUG
-
Given SC Q3W
- DRUG
-
Dosed per package label starting with 5 mg PO BID
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Pfizer CT.gov Call Center · Pfizer
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SEQUENTIAL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2020-09-24
- Primary Completion
- 2024-11-15
- Completion
- 2024-11-15
- FDA Drug
- Yes
Countries
- United States
- Canada
- Italy
- Japan
- Spain
Study Locations
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