Evaluation of the CHF 5993 concentration in blood, after inhalation with two different devices, (NEXThaler® versus pMDI), with and without Aerochamber spacer device, in healthy volunteers.

2024-512792-13-00 Protocol CLI-05993BB1-01 Human pharmacology (Phase I) - Other Ended

Start 13 Nov 2024 · End 17 Feb 2025 · Status Ended · 1 EU/EEA countries · 1 sites · Protocol CLI-05993BB1-01

Overview

Sponsor-declared trial summary

Phase Human pharmacology (Phase I) - Other
Status Ended
Participants planned 66
Countries 1
Sites 1

Asthma

Key facts

Sponsor
Chiesi Farmaceutici S.p.A.
Participant type
Healthy volunteers
Age range
18-64 years
Gender
Male and Female
Therapeutic area
Diseases [C] - Respiratory Tract Diseases [C08]
Trial duration
13 Nov 2024 → 17 Feb 2025
Decision date (initial)
2024-10-07
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

Asthma

Sponsors and contacts

Sponsor organisations, regulatory contacts, third parties

Chiesi Farmaceutici S.p.A.

Sponsor organisation
Chiesi Farmaceutici S.p.A.
Address
Via Palermo 26 A
City
Parma
Postcode
43122
Country
Italy

Scientific contact point

Organisation
Chiesi Farmaceutici S.p.A.
Contact name
- GLOBAL CLINICAL DEVELOPMENT

Public contact point

Organisation
Chiesi Farmaceutici S.p.A.
Contact name
- GLOBAL CLINICAL DEVELOPMENT

Locations

1 EU/EEA country · 1 investigational sites

By country

CountryMS statusPlanned subjectsSites
Belgium Ended 66 1
Rest of world 0

Investigational sites

Belgium

1 site · Ended
SGS Belgium
SGS Belgium NV – Clinical Pharmacology Unit, Drie Eikenstraat 655, 2650, Edegem

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 2024-11-13 2025-02-17 2024-11-13 2024-12-20

Application history

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

#TypeCodeSubmittedReference MSConclusionDecision date
1 INITIAL IN 2024-08-23 Belgium Acceptable
2024-10-07
2024-10-07
2 SUBSTANTIAL MODIFICATION SM-1 2024-10-08 Belgium Acceptable 2024-10-21