Chiesi Farmaceutici S.p.A.

30 total trials 4 currently recruiting 18 completed

Chiesi Farmaceutici S.p.A. sponsors 30 registered US clinical trials on ClinicalTrials.gov, 4 of them currently recruiting, and 18 completed. 9 of these trials are in Phase 3-4 (later-stage) and 15 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Fabry Disease, with 4 trials.

Trial Pipeline

30 total, page 1 of 1

RECRUITING Phase 2

A Study to Learn About the Safety and Effects of the Study Drug PRX-102 in Children and Adolescents With Fabry Disease

NCT06328608

RECRUITING

Maternal and Postnatal Outcomes Study (MOS): A Global Observational Registry Assessing the Safety of Elfabrio® in Women With Fabry Disease and Their Infants During Pregnancy and Breastfeeding

NCT06941025

RECRUITING

Analysis of Velmanase Alfa (Lamzede®)'s Effects in the Body of Children With Alpha-Mannosidosis Under the Age 3

NCT06184503

RECRUITING

A Multi-Country Observational Study of Safety and Effectiveness of Elfabrio® in Fabry Patients

NCT06663358

ACTIVE NOT RECRUITING Phase 3

Open Label Extension of 2 mg/kg Pegunigalsidase Alfa (PRX-102) Every 4 Weeks in Adult Fabry Disease Patients

NCT03614234

COMPLETED Phase 1

A Thorough QT (TQT) Study of CHF5993 pMDI in Healthy Volunteers (HV)

NCT05830071

COMPLETED Phase 3

A Study Testing the Superiority of CHF 1535 pMDI 800/24µg Total Daily Dose Compared With CHF 718 pMDI 800µg Total Daily Dose in Adults With Asthma on Medium or High-Dose Inhaled Corticosteroid

NCT05292586

COMPLETED Phase 3

A Study Comparing Efficacy, Safety and Tolerability of the Fixed Dose Triple Combination CHF 5993 With the Fixed Dose Dual Combination CHF 1535 in Subjects With COPD

NCT04320342

COMPLETED

Fabry Patient's Experience Of PegunigaLsidasE Alfa Monthly Infusion

NCT05186324

TERMINATED Phase 3

A 52-week, Placebo-controlled Study to Evaluate the Efficacy and Safety of 2 Doses of CHF6001 DPI (Tanimilast), as add-on to Maintenance Triple Therapy in Subjects With COPD and Chronic Bronchitis (PILASTER)

NCT04636801

TERMINATED Phase 3

A 52-week, Placebo- and Active- Controlled (Roflumilast, Daliresp® 500µg) Study to Evaluate the Efficacy and Safety of Two Doses of CHF6001 DPI (Tanimilast) as add-on to Maintenance Triple Therapy in Subjects With COPD and Chronic Bronchitis. (PILLAR)

NCT04636814

TERMINATED Phase 3

A Study in Preterm Neonates With Respiratory Distress Syndrome (RDS) Comparing CUROSURF® Administration Through Less Invasive Surfactant Administration (LISA) and Conventional Administration

NCT02772081

TERMINATED Phase 2

Poractant Alfa (Curosurf®)) -- Effect in Adult Patients Diagnosed With 2019 Novel Coronavirus (SARS-COV-19; (Covid-19)) Acute Respiratory Distress Syndrome (ARDS)

NCT04502433

TERMINATED Phase 2

CHF6563 in Babies With Neonatal Opioid Withdrawal Syndrome

NCT04104646

TERMINATED Phase 3

Efficacy and Safety of CUSA-081 in the Restoration of Central Venous Access Device (CVAD) Functionality

NCT03594175

COMPLETED

Registry Study of Revcovi Treatment in Patients With ADA-SCID

NCT03878069

COMPLETED Phase 3

Open Label Extension Study of 1 mg/kg Pegunigalsidase Alfa Every 2 Weeks in Patients With Fabry Disease

NCT03566017

COMPLETED Phase 2

A Dose Ranging Study With CHF 1531 in Subjects With Asthma (FLASH)

NCT03086460

COMPLETED Phase 2

A 6-week Dose Ranging Study of CHF 5259 pMDI in Subjects With Chronic Obstructive Pulmonary Disease

NCT03084796

COMPLETED Phase 2

An 8-week Dose Ranging Study of CHF 718 pMDI in Asthmatic Subjects

NCT03084718

COMPLETED Phase 1

Cangrelor Neonatal PK/PD and Safety Study

NCT02765633

COMPLETED Phase 2

A Double Blind, Randomized, Controlled Study to Evaluate CHF 5633 (Synthetic Surfactant) and Poractant Alfa in Neonates With Respiratory Distress Syndrome (RDS) (POC)

NCT02452476

COMPLETED

AssessmenT of smalL Airways involvemeNT In aSthma (ATLANTIS)

NCT02123667

TERMINATED Phase 4

Assessment of Efficacy, Safety and Dosing of Clevidipine in Pediatric Participants Undergoing Surgery (PIONEER)

NCT01938547

COMPLETED Phase 2

Evaluation of Safety & Tolerability of Multiple Dose Regimens of CHF 5074 and Exploration of Effects on Potential Markers of Clinical Efficacy in Patients With Mild Cognitive Impairment - Prolonged Open Label Extension Phase

NCT01602393

COMPLETED Phase 2

Evaluation of Safety & Tolerability of Multiple Dose Regimens of CHF 5074 and Exploration of Effects on Potential Markers of Clinical Efficacy in Patients With Mild Cognitive Impairment - Open Label Extension (CT04 OLEP)

NCT01421056

COMPLETED Phase 2

Safety and Efficacy Study of Treatment With Single Doses of CHF 4226 pMDI in Patients With Chronic Obstructive Pulmonary Disease (COPD)

NCT00782535

COMPLETED Phase 1

Evaluation of Possible Effects on the QTc Interval of CHF 4226 pMDI in Healthy Volunteers

NCT00777595

COMPLETED Phase 2

Confirmatory Dose Finding Study of 2 Dosages of CHF 4226 pMDI (Carmoterol) in Patients With COPD

NCT00640484

COMPLETED Phase 2

Dose Finding Study of CHF 4226 for Treating Patients With COPD

NCT00605891

Phase Distribution

PhaseTrial count
Phase 1 3
Phase 2 12
Phase 3 8
Phase 4 1

What the Pipeline for Chiesi Farmaceutici S.p.A. Shows

According to the ClinicalTrials.gov registry, Chiesi Farmaceutici S.p.A. is linked to 30 US clinical trials across every stage of research activity. Of those, 4 studies are currently recruiting, about 13% of the sponsor's indexed portfolio, and 18 are already marked complete, representing roughly 60% of the total.

The phase mix for Chiesi Farmaceutici S.p.A. reports 9 late-stage studies (Phase 3 and Phase 4 combined) and 15 earlier-phase studies (Phase 1 and Phase 2).

The top therapeutic focus area indexed for Chiesi Farmaceutici S.p.A. is Fabry Disease with 4 linked trials, and 5 other condition areas appear in the top list above.

How to read these pipeline numbers

Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.

A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work, safety, dosing, and early signal detection, and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.

That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice, verify current details directly with ClinicalTrials.gov before relying on any figure here.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page aggregates every registered trial from this sponsor, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.