Safety/PK Study of Gene Modified Donor T Cell Infusion in Children With Recurrent Hem Malignancies After Allo Transplant
A Phase I Study Of Safety, Pharmacokinetics, And Efficacy Of Donor BPX-501 Cells and Rimiducid Infusion For Children With Recurrent Hematologic Malignancies or Minimal Residual Disease After Allogeneic Transplant
Sponsor: Bellicum Pharmaceuticals
Listed as NCT03459170, this PHASE1 trial focuses on Hematologic Malignancy and remains ongoing. Sponsored by Bellicum Pharmaceuticals, it has been updated 11 times since 2018, reflecting substantial change activity. This study adds to the evidence base for this therapeutic area through structured, versioned documentation.
Status Flow
Change History
11 versions recorded-
Sep 2024 — Present [monthly]
Active Not Recruiting PHASE1
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Jul 2024 — Sep 2024 [monthly]
Active Not Recruiting PHASE1
-
Sep 2022 — Jul 2024 [monthly]
Active Not Recruiting PHASE1
-
Jan 2021 — Sep 2022 [monthly]
Active Not Recruiting PHASE1
-
Nov 2020 — Jan 2021 [monthly]
Active Not Recruiting PHASE1
Status: Recruiting → Active Not Recruiting
▶ Show 6 earlier versions
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Nov 2019 — Nov 2020 [monthly]
Recruiting PHASE1
-
Oct 2019 — Nov 2019 [monthly]
Recruiting PHASE1
-
Oct 2018 — Oct 2019 [monthly]
Recruiting PHASE1
-
Sep 2018 — Oct 2018 [monthly]
Recruiting PHASE1
-
Jun 2018 — Sep 2018 [monthly]
Recruiting PHASE1
-
Mar 2018 — Jun 2018 [monthly]
Recruiting PHASE1
First recorded
Feb 2018
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- Bellicum Pharmaceuticals
For direct contact, visit the study record on ClinicalTrials.gov .