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No longer availableNCT02955446Updated Feb 1, 2019

Compassionate Use Protocol for PF-03084014 in Patients With Advanced Solid Tumor Malignancies

An expanded access record providing PF-03084014 in Neoplasm and Desmoid Tumor, sponsored by University of Colorado, Denver. No longer available at 1 site in United States. Open to participants aged 16 Years to 101 Years. Per ClinicalTrials.gov, last updated 2019-02-01.

Sponsored by University of Colorado, Denver · Expanded access

Study type
Expanded access
Access type
Treatment IND/protocol
Ages
16 Years to 101 Years
Sex
All
01

Study summary

This is a single-center, open label, non randomized, compassionate use protocol in patients with advanced solid tumor malignancies who were previously enrolled in the phase I study (NCT00878189) of this agent.

Read the detailed description

This is an expanded access-physician sponsored trial of PF-03084014, a novel gamma-secretase inhibitor being developed for cancer therapy. This trial is designed for patients who have been on a previous Industry-sponsored phase I trial using PF-03084014 for> 1 year. The study is designed to evaluate the safety of prolonged oral administration of single agent PF-03084014. There are two study subjects with desmoid tumor who have been on the trial for a prolonged period of time (54 and 77 months, respectively) with either stable disease or response, indicating significant clinical benefit for a patient population in which there are few options. The goal of this protocol is to allow these subjects, who are clearly benefiting from PF-03084014, to continue to receive it

02

Conditions studied

  • Neoplasm
  • Desmoid Tumor

Keywords

  • Refractory Tumors
  • Advanced Solid Tumors
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In context

Fibromatosis, Aggressive

34 studies on the registry are indexed under Fibromatosis, Aggressive; 4 are open to participants now.

Browse Fibromatosis, Aggressive studies →

Lead sponsor

University of Colorado, Denver is the lead sponsor of 1,499 studies on the registry; 315 are open to participants now.

Of its 139 completed or terminated interventional studies of FDA-regulated products, 89 (64%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
16 Years to 101 Years
Sexes eligible
All

Inclusion criteria

  • Patients who are currently enrolled in A8641014 for > 1 year are eligible

Exclusion criteria

Exclusion Criteria:

  • Prior treatment with a gamma secretase inhibitor for treatment of cancer
  • Patients taking Tamoxifen
  • Patients with active graft versus host disease
  • Known human immunodeficiency virus (HIV) or acquired immunodeficiency syndrome (AIDS) related illness
  • Patients who are pregnant or breast-feeding
  • Patients with clinical evidence of central nervous system disease
05

Access details

Study type
Expanded access
Access type
Treatment IND/protocol

Available treatment

  • DrugPF-03084014

    Two patients enrolled in this study will continue receiving 80mg BID doses of PF-03084014, which was the same dose/schedule of their latest cycle on protocol A8641014. PF-03084014 will be administered twice a day in the morning and evening divided by approximately 12 hours. PF-03084014 should be administered in cycles of 21 days continuously.

    Also known as: Gamma Secretase Inhibitor

06

Where to request access

1 site
  • University of Colorado
    Aurora, Colorado 80045, United States
07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 1, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02955446
Lead sponsor
University of Colorado, Denver
Collaborators
SpringWorks Therapeutics, Inc.
Responsible party
Sponsor
First posted
Nov 4, 2016
Last update
Feb 1, 2019

Study contacts

Wells Messersmith, MD
principal investigator · University of Colorado, Denver
View the source record on ClinicalTrials.gov ↗

Requesting access

Expanded access is arranged between your doctor and the company. Ask your care team to contact the provider listed on this record.

No contact was published for this record. The registry link below has the sponsor’s details.

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