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NCT04152018 · ClinicalTrials.gov registry record · Phase 1

Study of PF-06940434 in Patients With Advanced or Metastatic Solid Tumors.

A Phase 1 study, sponsored by Pfizer.

Terminated
Registry status
Phase 1
Development phase
85
Enrollment target

NCT04152018: Clinical Trial Phase 1 study, sponsored by Pfizer.

NCT04152018 is a Phase 1 study that was terminated before completion, run by Pfizer. The registered enrollment target is 85 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (42% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04152018, a Phase 1 study, was terminated before completion, sponsored by Pfizer.

TERMINATED
Registry status
Phase 1
Development phase
85 participants
Enrollment target

Study Summary

Open-label, multi-center, non-randomized, multiple dose, safety, tolerability, pharmacokinetic, and pharmacodynamics and clinical activity study of PF-06940434 (Integrin alpha-V/beta-8 Antagonist) in patients with SCCHN (Squamous Cell Carcinoma of the Head and Neck), renal cell carcinoma (RCC - clear cell and papillary), ovarian, gastric, esophageal, esophageal (adeno and squamous), lung squamous cell, pancreatic and biliary duct, endometrial, melanoma and urothelial tumors. This study contains two parts, single agent dose escalation (Part 1A), dose finding of PF 06940434 in combination with anti-PD-1 (Part 1B) and dose expansion (Part 2). Part 2 Dose Combination Expansion will enroll participants into 3 cohorts at doses determined from Part 1B in order to further evaluate the safety of PF-06940434 in combination with anti-PD-1.

Interventions

  • DRUG PF-06801591
  • DRUG PF-06940434

Trial Details

FieldValue
Enrollment Target 85 participants
Start Date 2019-11-13
Est. Completion 2024-12-10
Phase Phase 1
Pfizer

1,845 total trials

Why NCT04152018 stopped before completion

NCT04152018 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 85 participants, a relatively small participant target, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (42% higher).

The record links to 0 conditions, and to 2 interventions - of which PF-06801591 is the first listed.

NCT04152018 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04152018 about?

NCT04152018 is a clinical study titled "Study of PF-06940434 in Patients With Advanced or Metastatic Solid Tumors.". Open-label, multi-center, non-randomized, multiple dose, safety, tolerability, pharmacokinetic, and pharmacodynamics and clinical activity study of PF-06940434 (Integrin alpha-V/beta-8 Antagonist) in patients with SCCHN (Squamous Cell Carcinoma of the Head and Neck), renal cell carcinoma (RCC - clea...

What is the current status of trial NCT04152018?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 85 participants. The study started on 2019-11-13. Estimated completion is 2024-12-10.

What interventions are being tested in trial NCT04152018?

The interventions under investigation include: PF-06801591 (DRUG), PF-06940434 (DRUG).

Who is sponsoring clinical trial NCT04152018?

This trial is sponsored by Pfizer, which has 1,845 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04152018's enrollment target sits among peer trials

85 656th of 2000 higher than 1,342 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT04152018, the US trial registry maintained by the National Library of Medicine. NCT04152018 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.