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NCT04691141: HATCH

A Study to Evaluating the Pharmacokinetics, Safety, and Efficacy of ATG 016 Monotherapy in IPSS-R Intermediate Risk and Above Myelodysplastic Syndrome (MDS)

Terminated Phase 1, PHASE2 Last updated 17 April 2024
What this trial tests

Phase 1, PHASE2 trial testing ATG-016 in Myelodysplastic Syndrome in 15 participants. Terminated before completion.

Timeline
23 February 2021
Primary endpoint
19 September 2023
19 September 2023

Quick facts

Lead sponsorShanghai Antengene Corporation Limited
PhasePhase 1, PHASE2
StatusTerminated
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment15
Start date23 February 2021
Primary completion19 September 2023
Estimated completion19 September 2023
Sites6 locations across China

Drugs / interventions tested

Conditions studied

Sponsor

Shanghai Antengene Corporation Limited — full company profile →

Who can join

18 and older, any sex, with Myelodysplastic Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a Phase Ⅰ/II, Open-label Study to Investigate the Pharmacokinetics, Safety, and Efficacyof ATG 016 Monotherapy in IPSS-R Intermediate Risk and above Myelodysplastic Syndrome (MDS) Patients after Failure of Hypomethylating Agent (HMA)-based Therapy.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Risk-Adapted, Individualized Treatment Strategies of Myelodysplastic Syndromes (MDS) and Chronic Myelomonocytic Leukemia (CMML).
    Bewersdorf JP, Zeidan AM. · · 2021 · cited 21× · PMID 33807279 · DOI 10.3390/cancers13071610

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Other trials of ATG-016

Trials testing the same drug.

Other recruiting trials for Myelodysplastic Syndrome

Currently open trials in the same condition.

Other Shanghai Antengene Corporation Limited trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04691141.

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