πŸ›οΈ Verified NIH Record β€’ Updated 2026-01-28

Evaluate BL-B01D1 in Patients With Metastatic or Unresectable Non-Small Cell Lung Cancer (NSCLC) and Other Solid Tumors (NCT05983432)

A Phase 1 Study Evaluating the Safety, Tolerability, and Efficacy of BL-B01D1 in Subjects With Metastatic or Unresectable Non-Small Cell Lung Cancer and Other Solid Tumors

🟒 Recruiting Phase1 πŸ’Š Investigational Drug / Biologic Sponsor: SystImmune Inc.

🩺 Plain-English Summary (8th-Grade Level)

The objective of this study is to evaluate the safety, tolerability, and efficacy of BL-B01D1 in patients with Metastatic or Unresectable Non-Small Cell Lung Cancer (NSCLC) and Other Solid Tumors.

Who can join: Review the eligibility criteria below.

Location: Beverly Hills Cancer Center β€” Beverly Hills, California

Age range: 18 Years

πŸ§ͺ Interventions in This Study

πŸ“‹ "Do I Qualify?" β€” 1-Minute Self Screener

Instant Checklist

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

πŸ“ All Participating Trial Locations (39 Sites)

Showing the first 25 of 39 sites.

  • Beverly Hills Cancer Center β€” Beverly Hills, California
  • City of Hope Cancer Center β€” Duarte, California
  • Chao Family Comprehensive Cancer Care and Ambulatory Care β€” Irvine, California
  • Chao Family Comprehensive Cancer Center and Ambulatory Care β€” Irvine, California
  • University of California Irvine Medical Center β€” Orange, California
  • UCLA Santa Monica β€” Santa Monica, California
  • University of Colorado Cancer Center β€” Aurora, Colorado
  • Yale University, Yale Cancer Center β€” New Haven, Connecticut
  • Georgetown University Medical Center β€” Washington D.C., District of Columbia
  • Sylvester Comprehensive Cancer Center β€” Miami, Florida
  • Sara Cannon Research Institute Lake Nona β€” Orlando, Florida
  • Hematology - Oncology Associates of the Treasure Coast β€” Port Saint Lucie, Florida
  • Northwestern University Feinberg School of Medicine β€” Chicago, Illinois
  • University of Iowa Hospital and Clinics β€” Iowa City, Iowa
  • Norton Cancer Institute β€” Louisville, Kentucky
  • Massachusetts General Hospital β€” Boston, Massachusetts
  • Dana-Farber Cancer Institute β€” Boston, Massachusetts
  • Memorial Sloan Kettering Cancer Center Head Neck Services β€” New York, New York
  • PRISMA Health/ITOR β€” Greenville, South Carolina
  • Sarah Cannon - Tennessee Oncology β€” Nashville, Tennessee
  • Oncology Consultants, P.A. β€” Houston, Texas
  • University of Texas M.D. Anderson Cancer Center β€” Houston, Texas
  • Virginia Cancer Specialists β€” Fairfax, Virginia
  • University of Washington Fred Hutchinson β€” Seattle, Washington
  • Centre LΓ©on BΓ©rard β€” Lyon,

πŸ“ž Contact the Study Coordinator

Phone: (425) 453-6841

Email: tara.barrineau@systimmune.com

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

πŸ’° 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 Β§ 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.

πŸ’‘ 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.
πŸ›οΈ View Official NIH Record β†—