TLN-121 in Relapsed or Refractory Non-Hodgkin Lymphomas (NCT07082803)
An Open-Label, Multicenter, Phase 1 Trial to Evaluate the Safety, Pharmacokinetics, and Anti-Tumor Activity of TLN-121 as a Single Agent and in Combination With Other Anti-Lymphoma Agents, in Patients With Relapsed or Refractory Non-Hodgkin Lymphomas
🩺 Plain-English Summary (8th-Grade Level)
The primary purpose of this study is to evaluate the safety, pharmacokinetics,, and preliminary anti-tumor activity of TLN-121 as a single agent and in combination with other anti-lymphoma therapies in patients with relapsed or refractory Non-Hodgkin Lymphomas
Who can join: Review the eligibility criteria below.
Location: Stanford Medicine Cancer Center — Palo Alto, California
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 (14 Sites)
- Stanford Medicine Cancer Center — Palo Alto, California
- The START Center for Cancer Care - Midwest — Grand Rapids, Michigan
- Washington University School of Medicine — St Louis, Missouri
- Memorial Sloan Kettering Cancer Center — New York, New York
- Weill Cornell Medicine - New York Presbyterian Hospital — New York, New York
- Hospital of the University of Pennsylvania — Philadelphia, Pennsylvania
- SCRI Oncology Partners — Nashville, Tennessee
- The University of Texas MD Anderson Cancer Center — Houston, Texas
- Macquarie University Hospital — Macquarie Park, New South Wales
- Princess Alexandra Hospital — Woolloongabba, Queensland
- Cabrini Health — Malvern, Victoria
- Peter MacCallum Cancer Centre — Melbourne, Victoria
- Linear Clinical Research — Perth, Western Australia
- BC Cancer - Vancouver — Vancouver, British Columbia
📞 Contact the Study Coordinator
Phone: (857) 228-0050
Email: clinicaloperations@treeline.bio
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.
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💡 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.