Randomized, double-blind, placebo-controlled, two-part study assessing the safety, tolerability and pharmacokinetics of BP1.7881 administered as higher doses, after single ascending doses (Part I) and multiple ascending doses (Part II), including the assessment of BP1.7881 on cardiac repolarization, in healthy subjects.

2024-512722-28-00 Protocol P22-03 Human pharmacology (Phase I) - Other Ongoing, recruiting

Start 22 Apr 2025 · Status Ongoing, recruiting · 1 EU/EEA countries · 1 sites · Protocol P22-03

Overview

Sponsor-declared trial summary

Phase Human pharmacology (Phase I) - Other
Status Ongoing, recruiting
Participants planned 161
Countries 1
Sites 1

Eosinophilic esophagitis

Key facts

Sponsor
Bioprojet Pharma
Participant type
Healthy volunteers
Age range
18-64 years
Gender
Male and Female
Therapeutic area
Diseases [C] - Immune System Diseases [C20]
Trial duration
22 Apr 2025 → ongoing
Decision date (initial)
2025-03-07
Transition trial
No
Low-intervention
No
Rare-disease indication
Yes
Vulnerable population
No

Trial design

CTIS Part I — objectives, methods, condition coding

Conditions and MedDRA coding

Eosinophilic esophagitis

VersionLevelCodeTermSystem organ class
20.1 PT 10064212 Eosinophilic oesophagitis 100000004856

Sponsors and contacts

Sponsor organisations, regulatory contacts, third parties

Bioprojet Pharma

Sponsor organisation
Bioprojet Pharma
Address
9 Rue Rameau
City
Paris
Postcode
75002
Country
France

Scientific contact point

Organisation
Bioprojet Pharma
Contact name
Clinical Development Director

Public contact point

Organisation
Bioprojet Pharma
Contact name
Clinical Development Director

Locations

1 EU/EEA country · 1 investigational sites

By country

CountryMS statusPlanned subjectsSites
Belgium Ongoing, recruiting 161 1
Rest of world 0

Investigational sites

Belgium

1 site · Ongoing, recruiting
Advanced Technology Corporation
CLINICAL PHARMACOLOGY UNIT, Avenue De L'hopital 1, Etage 2e Tour 2 Route 124, Liege

Country notifications

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

Country Trial startTrial end Recruitment startRecruitment end Early termination
Belgium 2025-04-22 2025-04-22

Application history

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

#TypeCodeSubmittedReference MSConclusionDecision date
1 INITIAL IN 2025-01-31 Belgium Acceptable
2025-03-07
2025-03-07
2 NON SUBSTANTIAL MODIFICATION NSM-1 2026-04-10 Belgium Acceptable
2025-03-07
2026-04-10