๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-05-05

A Study of CTX-009 in Combination With Paclitaxel in Adult Patients With Unresectable Advanced, Metastatic or Recurrent Biliary Tract Cancers (COMPANION-002) (NCT05506943)

A Phase 2/3 Randomized, Controlled Study of CTX-009 in Combination With Paclitaxel Versus Paclitaxel Alone in Adult Patients With Unresectable Advanced, Metastatic or Recurrent Biliary Tract Cancers Who Have Received One Prior Systemic Chemotherapy Regimen

๐Ÿ”ต Active, Not Recruiting Phase2 / Phase3 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: Compass Therapeutics

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

This is a multi-center, open-label, randomized, phase 2/3 trial of the bispecific antibody CTX-009 plus paclitaxel versus paclitaxel in patients with previously treated, unresectable advanced or metastatic biliary tract cancers.

Who can join: Review the eligibility criteria below.

Location: Mayo Clinic Arizona โ€” Phoenix, Arizona

Age range: 18 Years

๐Ÿงช Interventions in This Study

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ All Participating Trial Locations (34 Sites)

Showing the first 25 of 34 sites.

  • Mayo Clinic Arizona โ€” Phoenix, Arizona
  • University of Arizona โ€” Tucson, Arizona
  • University of Southern California Norris Comprehensive Cancer Center โ€” Los Angeles, California
  • Stanford Medicine Cancer Center โ€” Palo Alto, California
  • University of California San Francisco โ€” San Francisco, California
  • Rocky Mountain Cancer Centers, LLP โ€” Aurora, Colorado
  • University of Florida โ€” Gainesville, Florida
  • Mayo Clinic Jacksonville โ€” Jacksonville, Florida
  • AdventHealth Orlando โ€” Orlando, Florida
  • Northwestern University โ€” Chicago, Illinois
  • University of Chicago โ€” Chicago, Illinois
  • Ochsner Clinic Foundation โ€” New Orleans, Louisiana
  • Johns Hopkins University โ€” Baltimore, Maryland
  • Massachusetts General Hospital โ€” Boston, Massachusetts
  • Mayo Clinic Rochester โ€” Rochester, Minnesota
  • Washington University School of Medicine, Siteman Cancer Center โ€” St Louis, Missouri
  • Rutgers Cancer Institute โ€” New Brunswick, New Jersey
  • The University of New Mexico โ€” Albuquerque, New Mexico
  • Memorial Medical Center โ€” Las Cruces, New Mexico
  • Roswell Park โ€” Buffalo, New York
  • Columbia University โ€” New York, New York
  • Montefiore Medical Center โ€” The Bronx, New York
  • Gabrail Cancer Center โ€” Canton, Ohio
  • Cleveland Clinic โ€” Cleveland, Ohio
  • University of Tennessee Medical Center โ€” Knoxville, Tennessee

๐Ÿ“ž Contact the Study Coordinator

Phone: (800) 664-4580

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

๐Ÿ’ฐ 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 ยง 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.

๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
๐Ÿ›๏ธ View Official NIH Record โ†—