A Phase I Study of JL19001 Injection Alone or in Combination With Standard Therapy in Patients With Advanced Solid Tumors or Relapsed/Refractory B-cell Non-Hodgkin Lymphoma

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This is not medical advice. AI-assisted translation — inaccuracies may occur. Always verify the original and consult your oncologist before taking any steps.

About the trial

This is a Phase I, multicenter, single-arm, open-label clinical study designed to evaluate the safety and tolerability of JL19001 Injection as monotherapy (Phase Ia) or in combination with standard therapy (Phase Ib) in patients with AST and r/r B-NHL. Only the Phase Ia protocol design is registered at this time. A total of 6 dose cohorts are planned for Phase Ia, i.e., 1, 5, 10, 15, 20, and 25 μg/kg, with the administration route being subcutaneous injection. A traditional 3 + 3 dose escalation design will be used. The MTD and Recommended Maximum Add-on Dose (RMAD) for JL19001 Injection will be determined.

Original English text from ClinicalTrials.gov

Who can (and can't) join

✓ Qualifies

  • Wiek co najmniej 18 lat
  • Zaawansowany nowotwór litty lub chłoniak, który nie reaguje na standardowe leczenie, lub pacjent nie może go stosować
  • Wcześniejsze leczenie zgodnie z wymogami dla danego typu nowotworu
  • Dla czerniaków: progresja po co najmniej 2 liniach chemioterapii i immunoterapii
  • Dla raka nerki: przerzuty lub brak możliwości operacyjnego usunięcia guza
  • Dla raka płuc: stadium IV z progresją po co najmniej 2 liniach leczenia

Simplified criteria — AI translation

Trial details

Minimum age
18 Years
Last updated (source)
August 11, 2026
Sex
No restrictions

Therapies / drugs in trial

Locations (1)

Peking Union Medical College Hospital, Chinese Academy of Medical Sciences

Beijing, China

Trial contact

Contact information from ClinicalTrials.gov. Contact in English.

Share this trial

Data from ClinicalTrials.gov. AI-assisted translation, last sync: 8/11/2026.

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