CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 52 enrolled
Drug / intervention
AZD4573drug
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/NCT05140382
NCT05140382Phase 2Completed

A Modular Phase II, Open-label, Multicentre Study to Assess AZD4573 Efficacy and Safety as Monotherapy or in Combination With Anti-cancer Agents in Patients With Relapsed/Refractory Peripheral T-cell Lymphoma or Classical Hodgkin Lymphoma

AstraZeneca·interventional·Posted Dec 1, 2021·Updated Aug 28, 2024

In Brief

A Phase 2 clinical trial evaluating AZD4573 for Relapsed/Refractory Peripheral T-cell Lymphoma and Relapsed/Refractory Classical Hodgkins Lymphoma. Completed, enrolled 52 participants across 27 sites in 8 countries.

Detailed Summary

This is a modular dose confirmation and expansion study. The core study design is to assess the efficacy of AZD4573, administered as monotherapy or combination therapy, to participants with either r/r PTCL or r/r cHL and to confirm the safety profiles and PK in these populations. Module 1 of this study will evaluate the efficacy, safety, and tolerability of AZD4573 monotherapy in participants with r/r PTCL or r/r cHL. If AZD4573 monotherapy is found to have promising anti-tumour efficacy in Module 1, an AZD4573 monotherapy Phase II expansion may be added via a substantial protocol amendment.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesAustralia, France, Italy, South Korea, Sweden, Taiwan, United Kingdom, United States
Collaborators--

Timeline

Phase 2CompletedFinished
20222023202420252026
First PostedDec 1, 2021
Enrollment StartDec 15, 2021
Primary CompletionAug 25, 2023
Study CompletionFeb 16, 2024
TodayJul 2, 2026
Enrollment to primary: 1.7 yearsPosted 4.6 years ago

Interventions

AZD4573drug

AZD4573 will be given intravenously