Evaluation of GLR2007 for Advanced Solid Tumors

NCT04444427 · Status: COMPLETED · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 19

Last updated 2022-12-23

No results posted yet for this study

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

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04444427 on ClinicalTrials.gov