This is a Phase 1 Study to Evaluate the Safety of LTZ-301 in Patients With Non-Hodgkin Lymphoma

Recruiting Phase 1 Interventional Study
Non-Hodgkin Lymphoma Refractory/ Relapsed DLBCL - Diffuse Large B Cell Lymphoma Mantle Cell Lymphoma (MCL) Follicular Lymphoma ( FL) Marginal Zone Lymphoma (MZL)
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 1
Study type
Interventional
Purpose
Treatment
Participants needed
42 (estimated)
Sponsor
LTZ Therapeutics, Inc. · Industry
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About This Trial

This study is a first-in-human (FIH), Phase 1, multicenter, open-label study to determine the safety, tolerability, pharmacokinetics, pharmacodynamics, and evaluate the preliminary anti-tumor activity of LTZ-301 administered as a single agent in adult subjects with relapsed or refractory B-cell non-Hodgkin lymphoma

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Age ≥ 18 years * Relapsed or refractory to at least 2 prior systemic treatment regimens * At least 1 bi-dimensionally measurable lesion (≥ 1.5 cm) in longest dimension * Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1 * Adequate bone marrow, cardiac, pul…
Contacts

Sherry Unabia

669-207-0084

sherry.unabia@ltztherapeutics.com

CONTACT