Phase 1 clinical trial to evaluate the safety, tolerability and pharmacokinetics of multiple daily doses of IM-250 in healthy volunteers.

2024-519482-22-00 Protocol IM-102 Human pharmacology (Phase I) - Other Ended

Start 30 Apr 2025 · End 27 Jun 2025 · Status Ended · 1 EU/EEA countries · 1 sites · Protocol IM-102

Overview

Sponsor-declared trial summary

Phase Human pharmacology (Phase I) - Other
Status Ended
Participants planned 12
Countries 1
Sites 1

Healthy Volunteers

Key facts

Sponsor
Innovative Molecules GmbH
Participant type
Healthy volunteers
Age range
18-64 years
Gender
Male and Female
Therapeutic area
Not possible to specify
Trial duration
30 Apr 2025 → 27 Jun 2025
Decision date (initial)
2025-04-23
Transition trial
No
Low-intervention
No
Rare-disease indication
No
Vulnerable population
Yes

Trial design

CTIS Part I — objectives, methods, condition coding

Conditions and MedDRA coding

Healthy Volunteers

Sponsors and contacts

Sponsor organisations, regulatory contacts, third parties

Innovative Molecules GmbH

Sponsor organisation
Innovative Molecules GmbH
Address
Lipowskystrasse 10, Sendling Sendling
City
Munich
Postcode
81373
Country
Germany

Scientific contact point

Organisation
Innovative Molecules GmbH
Contact name
Company management

Public contact point

Organisation
Innovative Molecules GmbH
Contact name
Company management

Locations

1 EU/EEA country · 1 investigational sites

By country

CountryMS statusPlanned subjectsSites
Bulgaria Ended 12 1
Rest of world 0

Investigational sites

Bulgaria

1 site · Ended
Diagnostics And Consultation Center Convex Ltd.
Clinical Pharmacology, Ulitsa Sinanishko Ezero 11a, 1680, Sofiya

Country notifications

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

Country Trial startTrial end Recruitment startRecruitment end Early termination
Bulgaria 2025-04-30 2025-05-05 2025-06-27

Application history

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

#TypeCodeSubmittedReference MSConclusionDecision date
1 INITIAL IN 2025-01-24 Bulgaria Acceptable
2025-03-14
2025-04-23
2 NON SUBSTANTIAL MODIFICATION NSM-1 2025-05-02 Bulgaria Acceptable
2025-03-14
2025-05-02
3 NON SUBSTANTIAL MODIFICATION NSM-2 2025-05-12 Bulgaria Acceptable
2025-03-14
2025-05-12