Alzheimer Disease Clinical Trial
— SUVN-502Official title:
An Intermediate-Size, Expanded Access to SUVN-502 for the Treatment of Subjects With Alzheimer's Disease Who Have Completed the CTP2S1502HT6 Study
| NCT number | NCT03564964 |
| Other study ID # | EAP1502HT6 |
| Secondary ID | |
| Status | No longer available |
| Phase | |
| First received | |
| Last updated |
| Verified date | September 2020 |
| Source | Suven Life Sciences Limited |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Expanded Access |
This is an expanded access program (EAP) for eligible participants. This program is designed
to provide access to SUVN-502 for the treatment of Alzheimer's Disease. Investigator as well
as the subject/caregiver must decide whether the potential benefit outweighs the risk of
receiving an investigational therapy based on the patient's medical history and program
eligibility criteria.
Subjects will not be evaluated for efficacy and safety during the expanded access.
| Status | No longer available |
| Enrollment | 0 |
| Est. completion date | |
| Est. primary completion date | |
| Accepts healthy volunteers | |
| Gender | All |
| Age group | 50 Years to 85 Years |
| Eligibility |
Inclusion Criteria: - Subjects who have completed the 30 week treatment period of study CTP2S1502HT6 as planned and wish to continue treatment with SUVN-502. - Subject (or subject's legally acceptable representative) and caregiver must sign the Informed Consent Form (ICF) to participate in the study. Exclusion Criteria: - Has participated or is participating in any other clinical (investigational) study after completion of CTP2S1502HT6 study. - Is treated or likely to require treatment during the study with any medication prohibited by this expanded access program. |
| Country | Name | City | State |
|---|---|---|---|
| n/a | |||
| Lead Sponsor | Collaborator |
|---|---|
| Suven Life Sciences Limited |
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