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Our solutions

Pipeline

At Chiesi, our portfolio and pipeline are focused on developing and bringing to market innovative pharmaceutical solutions that improve quality of people’s life, with a strong focus on our core therapeutic areas: respiratory diseases, rare and ultra-rare diseases, neonatology, special and primary care.

This strategic choice allows us to continue expanding and strengthening our pipeline with studies that promise significant advancements for the future of our company, while also offering new opportunities for patients with unmet medical needs who currently lack therapeutic options for their conditions.

Respiratory diseases

Indication / Disease Active PrincipleFormulationRegionPhaseAlliance / Partnership
Asthma, COPDBDP + FFpMDI, DPIEUPost-approval-
Asthma, COPDBDP + FF + GBpMDI, DPIEUPost-approval-
Asthma, COPDBDP + FF + GBpMDI USPhase 3-
AsthmaBDP + FF + GBDPIEx USPhase 3-
Asthma, COPDBDP + FF + GBpMDI with HFA 152a (Carbon Minimal Inhaler)GlobalPhase 3-
Asthma, COPDBDP + FFpMDI with HFA 152a (Carbon Minimal Inhaler)GlobalPhase 3-
AsthmaBDPpMDI with HFA 152a (Carbon Minimal Inhaler)Selected countries in EU and Ex-EUPhase 3-
BronchiectasisDDP1iOralEx - ChinaPhase 3Haisco
BronchiectasisNEiDPIGlobalPhase 2-
Idiopathic pulmonary fibrosis (IPF)Zampilimab (anti TG-2)Intravenous (IV)-Phase 2UCB
Idiopathic pulmonary fibrosis (IPF)DDRiDPIGlobalPhase 1-

Rare diseases

Indication / DiseaseActive PrincipleFormulationRegionPhaseAlliance / Partnership
Alpha-mannosidosisVelmanase alfa-tycvLyophilized sterile powder for reconstitution with 5ml sterile water for infusionEU, USPost-approval-
Alpha-mannosidosis--GlobalPreclinicalKey2Brain
Krabbe disease--GlobalPreclinicalKey2Brain
Nephropathic cystinosisCysteamine bitartrateGastro-resistant hard capsulesEU, USPost-approvalAmgen
Fabry diseasePegunigalsidase alfa-iwxjIV SolutionEU, UK, USPost-approvalProtalix Biotherapeutics
Fabry disease - pediatricPegunigalsidase alfa-iwxjIV SolutionGlobalPhase 2/3Protalix Biotherapeutics
Fabry diseasePegunigalsidase alfa-iwxjIV SolutionJapanPhase 2/3Protalix Biotherapeutics
Other inborn errors of metabolism diseases--GlobalPreclinicalAliada
Leber’s Hereditary Optic Neuropathy (LHON)IdebenoneFlm-coated tabletsEUPost-approval-
Generalized LipodystrophyMetreleptinInjectionGlobalPost-approval-
Partial LipodystrophyMetreleptinInjectionEUPost-approval-
Partial LipodystrophyMetreleptinInjectionUSPhase 3-
AcromegalyOctreotideGastro-resistant hard capsulesUSPost-approval-
Homozygous Familial Hypercholesterolemia (HoFH)LomitapideCapsulesEU, USPost-approval-
Primary Hyperoxalurlia type 1--GlobalPhase 1/2Arbor Biotechnologies
Epidermolysis Bullosa (EB)Birch triterpenesTopical gelEU, USPost-approval-
Epidermolysis Bullosa (EB)Birch triterpenesTopical gelJapanPhase 3-
ThalassemiaDeferiproneTablets oral solutionEU, USPost-approval-
Sickle Cell Disease or Other AnaemiasDeferiproneTablets oral solutionUSPost-approval-
Adenosine Deaminase - Severe Combined Immune DeficiencyElapegademase-lvlrInjectionJP, USPost-approval-
Other rare diseases--GlobalPreclinicalArbor Biotechnologies



Special care and Primary care

Indication / DiseaseActive PrincipleFormulationRegionPhaseAlliance / Partnership
Neonatal RDS treatmentPoractant alfaEndotracheopulmonary Instillation sterile Suspension-Post-approval-
Treatment of primary apnoea of premature newbornsCaffeine CitrateSolution for infusion, oral solution-Post-approval-
Reduction of blood pressure when oral therapy is not feasible or in perioperative settingsClevidipineEmulsion-Post-approval-
Anti-platelet; reducing risk of thrombotic cardiovascular events undergoing percutaneous coronary intervention (PCI)CangrelorLyophilized powderUS, EUPost-approval-
Prophylaxis of transplant rejection in adult kidney or liver allograft recipientsTacrolimusProlonged-release tablets-Post-approvalVeloxis
Prevention of bronchopulmonary dysplasia (BPD)IGF-1 BiologicSterile solution for infusion-Phase 2bOak Hill Bio
Treatment of intestinal malabsorption in preterm infantsInsulinOral solution-Phase 3Elgan