Study of PF-07248144 in Advanced or Metastatic Solid Tumors (NCT04606446)
A PHASE 1/2A DOSE ESCALATION AND EXPANSION STUDY TO EVALUATE SAFETY, TOLERABILITY, PHARMACOKINETIC, PHARMACODYNAMIC, AND ANTI-TUMOR ACTIVITY OF PF-07248144 IN PARTICIPANTS WITH ADVANCED OR METASTATIC SOLID TUMORS
🩺 Plain-English Summary (8th-Grade Level)
This is an open-label, multi center study to evaluate safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of PF-07248144 and early signs of clinical efficacy of PF-07248144 as a single agent and in combination with other agents
Who can join: Review the eligibility criteria below.
Location: HonorHealth — Scottsdale, Arizona
Age range: 18 Years
🧪 Interventions in This Study
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (44 Sites)
Showing the first 25 of 44 sites.
- HonorHealth — Scottsdale, Arizona
- Cedars Sinai Medical Center — Los Angeles, California
- Cedars-Sinai Cancer at Cedars-Sinai Medical Center — Los Angeles, California
- UCSF Medical Center at Mission Bay — San Francisco, California
- Smilow Cancer Hospital at Yale - New Haven — New Haven, Connecticut
- Yale-New Haven Hospital- Yale Cancer Center — New Haven, Connecticut
- Smilow Cancer Hospital Phase 1 Unit — New Haven, Connecticut
- Yale University — New Haven, Connecticut
- Holy Cross Hospital — Fort Lauderdale, Florida
- St. Elizabeth Healthcare — Edgewood, Kentucky
- University Medical Center, lnc.:DBA University of Louisville Hospital — Louisville, Kentucky
- University of Louisville — Louisville, Kentucky
- UofL Health Brown Cancer Center — Louisville, Kentucky
- SCRI Oncology Partners — Nashville, Tennessee
- MD Anderson The Woodlands — Conroe, Texas
- The University of Texas M. D. Anderson Cancer Center — Houston, Texas
- U.T. MD Anderson Cancer Center — Houston, Texas
- MD Anderson West Houston — Houston, Texas
- MD Anderson League City — League City, Texas
- NEXT Oncology — San Antonio, Texas
- MD Anderson — Sugar Land, Texas
- Swedish Cancer Institute — Seattle, Washington
- Swedish Medical Center — Seattle, Washington
- Chris O'Brien Lifehouse — Camperdown, New South Wales
- Cancer Research South Australia — Adelaide, South Australia
📞 Contact the Study Coordinator
Phone: (800) 718-1021
Email: ClinicalTrials.gov_Inquiries@pfizer.com
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
Explore by condition: All Locally Advanced or Metastatic ER+ HER2- Breast Cancer clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.