Evaluation of GLR2007 for Advanced Solid Tumors
NCT04444427 · Status: COMPLETED · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 19
Last updated 2022-12-23
Summary
Evaluation of GLR2007 for Advanced Solid Tumors
Conditions
Interventions
- DRUG
-
GLR2007
Administered orally, once daily for 21 days followed by a 7-day treatment holiday.
Sponsors & Collaborators
-
Gan and Lee Pharmaceuticals, USA
lead INDUSTRY
Principal Investigators
-
Kimberly Lazaroff, MSN · Gan and Lee Pharmaceuticals, USA Corp
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SEQUENTIAL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2020-07-15
- Primary Completion
- 2022-07-29
- Completion
- 2022-07-29
- FDA Drug
- Yes
Countries
- United States
Study Locations
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