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RECRUITING
NCT05683717
PHASE1

A Phase 1 Study to Evaluate the Safety and Tolerability of TT-01488 in Patients With B-Cell Malignancies

Sponsor: TransThera Sciences (Nanjing), Inc.

View on ClinicalTrials.gov

Summary

This is a multicenter, open-label Phase I dose escalation study to evaluate the safety and preliminary efficacy of the TT-01488 tablet, a non-covalent reversible BTK inhibitor, for the treatment of adult patients with B-cell malignancies.

Official title: A Phase I, Multicenter, Open Label, and Dose-Escalation Study of TT-01488, Administered Orally in Adult Patients With B-Cell Malignancies

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

37

Start Date

2023-03-30

Completion Date

2028-10-30

Last Updated

2023-11-21

Healthy Volunteers

No

Interventions

DRUG

TT-01488 Tablets

TT-01488 tablet will be administered orally once daily per protocol defined schedule.

Locations (1)

The First Affiliated Hospital with Nanjing Medical University

Nanjing, Jiangsu, China