Busulfan Monotherapy as Conditioning for Autologous Hematopoietic Progenitor Cell Transplantation
A Pilot Study of Intravenous, Targeted-Dose Busulfan Monotherapy as Conditioning for Autologous Hematopoietic Progenitor Cell Transplantation in High-Risk AML
Sponsor: ESP Pharma
Terminated
Low accrual
Other Acute Myeloid Leukemia (AML) trials with similar outcome
Listed as NCT00363467, this NA trial focuses on Acute Myeloid Leukemia (AML) and remains terminated or withdrawn. Sponsored by ESP Pharma, it has been updated 6 times since 2006, reflecting limited change activity. This study contributes to the evolving evidence base for cancer treatment protocols.
Status Flow
Change History
6 versions recorded-
Sep 2024 — Present [monthly]
Terminated NA
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Jul 2024 — Sep 2024 [monthly]
Terminated NA
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Dec 2021 — Jul 2024 [monthly]
Terminated NA
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Jan 2021 — Dec 2021 [monthly]
Terminated NA
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Jun 2018 — Jan 2021 [monthly]
Terminated NA
▶ Show 1 earlier version
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Jan 2017 — Jun 2018 [monthly]
Terminated NA
First recorded
May 2006
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- ESP Pharma
- H. Lee Moffitt Cancer Center and Research Institute
For direct contact, visit the study record on ClinicalTrials.gov .