PainCart Study Evaluating the Analgesic Profile of SAGE-319

2025-521380-12-00 Protocol 319-TRM-101 Human pharmacology (Phase I) - Other Ended

Start 2 Jun 2025 · End 17 Jun 2025 · Status Ended · 1 EU/EEA countries · 1 sites · Protocol 319-TRM-101

Overview

Sponsor-declared trial summary

Phase Human pharmacology (Phase I) - Other
Status Ended
Participants planned 24
Countries 1
Sites 1

Disorders characterized by a deficit in GABAergic signaling and cerebellar circuitry.

Key facts

Sponsor
Sage Therapeutics Inc.
Participant type
Healthy volunteers
Age range
18-64 years
Gender
Male and Female
Therapeutic area
Psychiatry and Psychology [F] - Mental Disorders [F03]
Trial duration
2 Jun 2025 → 17 Jun 2025
Decision date (initial)
2025-05-30
Transition trial
No
Low-intervention
No
Rare-disease indication
No
Vulnerable population
No

Trial design

CTIS Part I — objectives, methods, condition coding

Conditions and MedDRA coding

Disorders characterized by a deficit in GABAergic signaling and cerebellar circuitry.

Sponsors and contacts

Sponsor organisations, regulatory contacts, third parties

Sage Therapeutics Inc.

Sponsor organisation
Sage Therapeutics Inc.
Address
55 Cambridge Pkwy
City
Cambridge
Postcode
02142-1234
Country
United States

Scientific contact point

Organisation
Sage Therapeutics Inc.
Contact name
Centre for Human Drug Research

Public contact point

Organisation
Sage Therapeutics Inc.
Contact name
Centre for Human Drug Research

Locations

1 EU/EEA country · 1 investigational sites

By country

CountryMS statusPlanned subjectsSites
Netherlands Ended 24 1
Rest of world 0

Investigational sites

Netherlands

1 site · Ended
Centre for Human Drug Research
Pain, Zernikedreef 8, 2333 CL, Leiden

Country notifications

Trial-start, recruitment-start, end and early-termination notifications submitted per Member State

Country Trial startTrial end Recruitment startRecruitment end Early termination
Netherlands 2025-06-02 2025-06-05

Application history

1 submissions — initial application plus substantial / non-substantial modifications

#TypeCodeSubmittedReference MSConclusionDecision date
1 INITIAL IN 2025-04-14 Netherlands Acceptable
2025-05-30
2025-05-30