CI

At a glance

ClinicalIndex Comparison Record
Phase 2Recruiting· 30 target
Drug / intervention
TGRX-814drug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT06206174
NCT06206174Phase 2RecruitingUpdate OverdueUpdated 26mo ago · Completion was 16mo ago
Enrollment Stalled
Update Overdue

A Single-arm, Open-label, Dose Escalation and Expansion Phase I/II Study Evaluating Safety, Tolerability, Pharmacokinetics and Preliminary Efficacy of TGRX-814 Monotherapy and Combination Therapy in Patients With Hematological Malignancies

Shenzhen TargetRx Co., Ltd.·interventional·Posted Jan 16, 2024·Updated Apr 10, 2024

In Brief

A Phase 2 clinical trial evaluating TGRX-814 for Hematologic Malignancy and 4 related conditions. Currently recruiting, targeting 30 participants across 1 site.

Signals

Enrollment appears stalled

Detailed Summary

The purpose of this single- arm, open-label, dose escalation and dose expansion phase I/II study is to evaluate the safety, tolerability, pharmacokinetic and preliminary efficacy of TGRX-814 in patients with hematological malignancies including non-Hodgkin lymphoma, acute myeloid leukemia, aute lymphoblastic leukemia and myelodysplastic syndromes.

Study Details

Timeline

Phase 2Recruiting
202420252026202720282029
First PostedJan 16, 2024
Enrollment StartMar 6, 2024
Primary CompletionFeb 28, 2025
Study CompletionFeb 28, 2029
TodayJul 1, 2026
Enrollment to primary: 12 monthsPosted 2.5 years ago

Interventions

TGRX-814drug

Participants are given TGRX-814 tablets for oral, once daily administration at one of the dose levels as pre-determined for the dose escalation sequence.