A study of the safety, absorption and effects of investigational drug ARV-102 in patients with Parkinson's disease.

2024-516888-84-00 Protocol ARV-102-103 Human pharmacology (Phase I) - Other Ended

Start 12 Nov 2024 · End 23 Dec 2025 · Status Ended · 1 EU/EEA countries · 1 sites · Protocol ARV-102-103

Overview

Sponsor-declared trial summary

Phase Human pharmacology (Phase I) - Other
Status Ended
Participants planned 44
Countries 1
Sites 1

Parkinson's disease.

Key facts

Sponsor
Arvinas Operations Inc.
Participant type
Patients
Age range
18-64 years, 65+ years
Gender
Male and Female
Therapeutic area
Phenomena and Processes [G] - Musculoskeletal and Neural Physiological Phenomena [G11]
Trial duration
12 Nov 2024 → 23 Dec 2025
Decision date (initial)
2024-10-29
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

Parkinson's disease.

Sponsors and contacts

Sponsor organisations, regulatory contacts, third parties

Arvinas Operations Inc.

Sponsor organisation
Arvinas Operations Inc.
Address
5 Science Park
City
New Haven
Postcode
06511-1966
Country
United States

Scientific contact point

Organisation
Arvinas Operations Inc.
Contact name
Clinical Trials NS

Public contact point

Organisation
Arvinas Operations Inc.
Contact name
Clinical Trials NS

Locations

1 EU/EEA country · 1 investigational sites

By country

CountryMS statusPlanned subjectsSites
Netherlands Ended 44 1
Rest of world 0

Investigational sites

Netherlands

1 site · Ended
Centre for Human Drug Research
Neurology, 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 2024-11-12 2025-12-23 2024-12-06 2025-12-23

Application history

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

#TypeCodeSubmittedReference MSConclusionDecision date
1 INITIAL IN 2024-09-16 Netherlands Acceptable
2024-10-29
2024-10-29
2 SUBSTANTIAL MODIFICATION SM-1 2025-05-13 Netherlands Acceptable
2025-06-24
2025-06-26
3 NON SUBSTANTIAL MODIFICATION NSM-1 2025-07-03 Netherlands Acceptable
2025-06-24
2025-07-03
4 NON SUBSTANTIAL MODIFICATION NSM-2 2025-07-18 Netherlands Acceptable
2025-06-24
2025-07-18