A study to examine the effects of oral NTX-1955 on the brain in healthy adults.

2025-521829-32-00 Protocol NTX-1955-101 Human pharmacology (Phase I) - Other Ended

Start 24 Jun 2025 · End 22 Dec 2025 · Status Ended · 1 EU/EEA countries · 1 sites · Protocol NTX-1955-101

Overview

Sponsor-declared trial summary

Phase Human pharmacology (Phase I) - Other
Status Ended
Participants planned 18
Countries 1
Sites 1

Generalized Anxiety Disorder (GAD)

Key facts

Sponsor
Newleos 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
24 Jun 2025 → 22 Dec 2025
Decision date (initial)
2025-06-24
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

Generalized Anxiety Disorder (GAD)

Sponsors and contacts

Sponsor organisations, regulatory contacts, third parties

Newleos Therapeutics Inc.

Sponsor organisation
Newleos Therapeutics Inc.
Address
501 Boylston Street Floor 10
City
Boston
Postcode
02116-3769
Country
United States

Scientific contact point

Organisation
Newleos Therapeutics Inc.
Contact name
Gabriel Jacobs

Public contact point

Organisation
Newleos Therapeutics Inc.
Contact name
Gabriel Jacobs

Locations

1 EU/EEA country · 1 investigational sites

By country

CountryMS statusPlanned subjectsSites
Netherlands Ended 18 1
Rest of world 0

Investigational sites

Netherlands

1 site · Ended
Centre for Human Drug Research
Psychiatry, 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 2025-06-24 2025-12-22 2025-07-02

Application history

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

#TypeCodeSubmittedReference MSConclusionDecision date
1 INITIAL IN 2025-05-02 Netherlands Acceptable
2025-06-19
2025-06-24
2 SUBSTANTIAL MODIFICATION SM-1 2025-08-18 Netherlands Acceptable
2025-09-16
2025-09-16