CI

At a glance

ClinicalIndex Comparison Record
Early Ph 1Not Yet Recruiting· 20 target
Drug / intervention
ALT001drug
Likely dose
ALT001 8 mLfrom record
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Search/NCT07514923
NCT07514923Early Ph 1Not Yet Recruiting

The Study of Safety and Preliminary Efficacy of ALT001 in Patients With MultIple System Atrophy-Cerebellar Type

yilong Wang·interventional·Posted Apr 7, 2026·Updated Apr 7, 2026

In Brief

A Early Phase 1 clinical trial evaluating ALT001 for Multiple System Atrophy - Cerebellar Subtype (MSA-C). Not yet recruiting, targeting 20 participants across 1 site.

Detailed Summary

This is a single-center, prospective, randomized, open-label, blinded outcome assessment (PROBE) study. At the end of the PROBE study, patients who have completed the study may opt to enter the open-label extension (OLE) study. The objective of the study is to evaluate the safety, tolerability and potential preliminary efficacy of ALT001 in the treatment of patients with multiple system atrophy-cerebellar type (MSA-C).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesChina
Collaborators--

Timeline

Early Ph 1Not Yet Recruiting
2027
First PostedApr 7, 2026
Enrollment StartApr 6, 2026
Primary CompletionJan 31, 2027
Study CompletionOct 30, 2027
TodayJul 1, 2026
Enrollment to primary: 10 monthsPosted 3 months agoPrimary completion in 7 months

Interventions

ALT001drug

Intrathecal administration combined with intravenous administration of ALT001 was given to each MSA patient in the intervention group, with intrathecal administration on days 1, 31 and 61 and intravenous administration on days 2 to 14, 32 to 44±3 and 62 to 74±5, and treatment was given once a day. intrathecal administration: 8 mL sodium chloride injection + ALT001 (130 μg/branch) for intrathecal administration, which was completed in about 5 minutes; intravenous administration: ALT001 (130 μg/branch) was dissolved in 100 ml sodium chloride injection, which was completed in about 30-40 minutes. After completion of the above treatments and 90±7 days of follow-up, all subjects entered the OLE study phase. During this period, all participants were given the option of continuing to receive 3 phases (on Days 91 to 104±7, Days 121 to 134±7, and Days 151 to 164±7) of intravenous ALT001 administration (14 consecutive days of ALT001 130 μg qd i.v. in each phase).