deltatrials
Terminated PHASE1 INTERVENTIONAL 1-arm NCT06388759

TQ05105 Tablet for Myelofibrosis Treatment in Ruxolitinib-Resistant or Intolerant Patients

A Phase Ib Study of TQ05105 Tablets for the Treatment of Intermediate and High Risk Myelofibrosis Refractory/Relapsed/Intolerant to Ruxolitinib

Sponsor: Chia Tai Tianqing Pharmaceutical Group Co., Ltd.

Conditions Myelofibrosis
Interventions TQ05105 Tablets
Updated 4 times since 2024 Last updated: Aug 24, 2025 Started: Aug 1, 2022 Primary completion: Aug 12, 2025 Completion: Aug 12, 2025
This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

Terminated

This study was closed due to business reasons. Closure was not prompted by any safety or efficacy concerns.

A PHASE1 clinical study on Myelofibrosis, this trial is terminated or withdrawn. The trial is conducted by Chia Tai Tianqing Pharmaceutical Group Co., Ltd. and has accumulated 4 data snapshots since 2022. Longitudinal tracking of this trial contributes to a broader understanding of treatment development timelines.

Status Flow

~May 2024 – ~Jul 2024 · 2 months · monthly snapshot~Jul 2024 – ~Sep 2024 · 2 months · monthly snapshot~Sep 2024 – ~Sep 2025 · 12 months · monthly snapshotActive Not Recruiting~Sep 2025 – present · 11 months · monthly snapshotTerminated

Change History

4 versions recorded
  1. Sep 2025 — Present [monthly]

    Terminated PHASE1

    Status: Active Not RecruitingTerminated

  2. Sep 2024 — Sep 2025 [monthly]

    Active Not Recruiting PHASE1

  3. Jul 2024 — Sep 2024 [monthly]

    Active Not Recruiting PHASE1

  4. May 2024 — Jul 2024 [monthly]

    Active Not Recruiting PHASE1

    First recorded

Aug 2022

Trial started

Per CT.gov start date — pre-dates our first snapshot

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:
  • Chia Tai Tianqing Pharmaceutical Group Co., Ltd.
Data source: Chia Tai Tianqing Pharmaceutical Group Co., Ltd.

For direct contact, visit the study record on ClinicalTrials.gov .