To Evaluate Safety, Tolerability and Pharmacological Effects of PU AD in Subjects With Mild AD Dementia
A Phase 2A Study to Evaluate Safety, Tolerability and Pharmacological Effects of PU AD in Subjects With Mild Alzheimer's Disease (AD) Dementia
Sponsor: Samus Therapeutics, Inc.
Terminated
Samus Therapeutics company closure
Other terminated trials from Samus Therapeutics, Inc.
- Post-Essential Thrombocythemia Myelofibrosis (Post-ET MF) · Phase PHASE1 · Nov 2022
- Glioblastoma Surgery · Phase PHASE1 · Nov 2022
- Myelofibrosis · Phase PHASE1 · Mar 2020
- Alzheimer's Disease · Phase PHASE1 · Dec 2019
More terminations from Samus Therapeutics, Inc.
Other Alzheimer Disease trials with similar outcome
Listed as NCT04311515, this PHASE2 trial focuses on Alzheimer Disease and remains terminated or withdrawn. Sponsored by Samus Therapeutics, Inc., it has been updated 12 times since 2020, reflecting substantial change activity. This study adds to the evidence base for this therapeutic area through structured, versioned documentation.
Status Flow
Change History
12 versions recorded-
Sep 2025 — Present [monthly]
Terminated PHASE2
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Sep 2024 — Sep 2025 [monthly]
Terminated PHASE2
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Jul 2024 — Sep 2024 [monthly]
Terminated PHASE2
-
Dec 2022 — Jul 2024 [monthly]
Terminated PHASE2
Status: Suspended → Terminated
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Sep 2022 — Dec 2022 [monthly]
Suspended PHASE2
Status: Terminated → Suspended
▶ Show 7 earlier versions
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Jun 2022 — Sep 2022 [monthly]
Terminated PHASE2
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May 2022 — Jun 2022 [monthly]
Terminated PHASE2
Status: Active Not Recruiting → Terminated
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Jan 2021 — May 2022 [monthly]
Active Not Recruiting PHASE2
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Nov 2020 — Jan 2021 [monthly]
Active Not Recruiting PHASE2
Status: Recruiting → Active Not Recruiting
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Sep 2020 — Nov 2020 [monthly]
Recruiting PHASE2
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Aug 2020 — Sep 2020 [monthly]
Recruiting PHASE2
Status: Not Yet Recruiting → Recruiting
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Apr 2020 — Aug 2020 [monthly]
Not Yet Recruiting PHASE2
First recorded
Eligibility Summary
No eligibility information available.
Contact Information
- Samus Therapeutics, Inc.
For direct contact, visit the study record on ClinicalTrials.gov .