A Phase 1 Study of ZE50-0134 in Relapsed and Refractory Chronic Lymphocytic Leukemia, Small Lymphocytic Lymphoma, and Select Low-grad Lymphomas

Part of paid clinical trials in Louisville, Kentucky.

Sponsor
Lomond Therapeutics Holdings, Inc.
Study ID
NCT06708897
Phase
PHASE1
Status
Recruiting

Conditions

  • CLL (Chronic Lymphocytic Leukemia)
  • CLL / SLL
  • SLL (Small Lymphocytic Lymphoma)

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • ZE 50-0134 — DRUG
    oral capsules QD

Study Details

This is a clinical study aiming to evaluate the safety, pharmacokinetics, pharmacodynamics, and preliminary efficacy of ZE50-0134 in relapsed and refractory chronic lymphocytic leukemia, small lymphocytic lymphoma, and select low-grad lymphomas.

Key Dates

Start date
Apr 8, 2025
Status verified
Nov 2025
Primary completion
Mar 31, 2026
Completion
Apr 30, 2028

Study Design

Enrollment
66 participants (estimated)
Allocation
NON_RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
TREATMENT

Arms

  • Experimental: ZE50-0134 Dose Level -1
    Optional and would only be performed Dose Level 1 is poorly tolerated
  • Experimental: ZE50-0134 Dose Level 1
  • Experimental: ZE50-0134 Dose Level 2
  • Experimental: ZE50-0134 Dose Level 3
  • Experimental: ZE50-0134 Dose Level 4
  • Experimental: ZE50-0134 Dose Level 5
  • Experimental: ZE50-0134 Selected dose 1
    The doses used in Part 2 of the study will be determined based on the data from Part 1 of the study
  • Experimental: ZE50-0134 Selected dose 2
    The doses used in Part 2 of the study will be determined based on the data from Part 1 of the study

Primary Outcome Measure

Incidence of AEs and SAEs [ Time Frame: Up to 24 cycles, 4 weeks each ]

Central Contacts

Locations (4)

FacilityCityStateZIPSite coordinators
Norton Cancer Institute, St. Matthews CampusLouisvilleKentucky40207-
University of North Carolina at Chapel HillChapel HillNorth Carolina27599-
University of CincinnatiCincinnatiOhio45221-
The Ohio State UniversityColumbusOhio43210-

Find similar trials in Louisville, KY

Related Studies