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
π©Ί 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
π§ͺ Interventions in This Study
π "Do I Qualify?" β 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria β
π 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,
π 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.
π° 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.
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π‘ 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.