Pharmacokinetics, pharmacodynamics, safety, and tolerability of an acetonic milk thistle extract, standardized to silymarin, in subjects with MASLD

2025-522423-95-00 Protocol SilMAKin Human pharmacology (Phase I) - Other Ongoing, recruiting

Start 14 Jan 2026 · Status Ongoing, recruiting · 1 EU/EEA countries · 1 sites · Protocol SilMAKin

Overview

Sponsor-declared trial summary

Phase Human pharmacology (Phase I) - Other
Status Ongoing, recruiting
Participants planned 48
Countries 1
Sites 1

chronic liver disease

Key facts

Sponsor
Bionorica SE
Participant type
Patients
Age range
18-64 years, 65+ years
Gender
Male and Female
Therapeutic area
Diseases [C] - Nutritional and Metabolic Diseases [C18]
Trial duration
14 Jan 2026 → ongoing
Decision date (initial)
2025-11-17
Transition trial
No
Low-intervention
No
Rare-disease indication
No
Vulnerable population
No

External identifiers

EU CT number
2025-522423-95-00
WHO UTN
U1111-1325-0199

Trial design

CTIS Part I — objectives, methods, condition coding

Conditions and MedDRA coding

chronic liver disease

Sponsors and contacts

Sponsor organisations, regulatory contacts, third parties

Bionorica SE

Sponsor organisation
Bionorica SE
Address
Kerschensteinerstrasse 11-15
City
Neumarkt I.D.Opf.
Postcode
92318
Country
Germany

Scientific contact point

Organisation
Bionorica SE
Contact name
Bernd Röther

Public contact point

Organisation
Bionorica SE
Contact name
Bernd Röther

Locations

1 EU/EEA country · 1 investigational sites

By country

CountryMS statusPlanned subjectsSites
Germany Ongoing, recruiting 48 1
Rest of world 0

Investigational sites

Germany

1 site · Ongoing, recruiting
CRS Clinical Research Services Mannheim GmbH
Clinic, Grenadierstrasse 1, Neckarstadt, Mannheim

Country notifications

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

Country Trial startTrial end Recruitment startRecruitment end Early termination
Germany 2026-01-14 2026-01-19

Application history

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

#TypeCodeSubmittedReference MSConclusionDecision date
1 INITIAL IN 2025-10-10 Germany Acceptable
2025-11-12
2025-11-17
2 SUBSTANTIAL MODIFICATION SM-1 2025-12-05 Germany Acceptable 2025-12-12
3 SUBSTANTIAL MODIFICATION SM-2 2026-03-05 Germany Acceptable
2026-03-18
2026-03-19