Close-up of a doctor holding a patient's hand in the consultation, reflecting the Ferrer company's commitment to health.

R & D

Clinical research

At Ferrer, science, empathy and innovation come together to transform lives

At Ferrer we promote rigorous clinical trials with the aim of transforming scientific knowledge into solutions that improve the lives of people with unmet medical needs. These studies are essential to advance new therapeutic options and improve the approach to diseases.

 

Through our clinical trials, we generate solid evidence on the safety, efficacy and value of our investigational treatments, contributing to informed decision-making by health authorities, health professionals and health systems.

A laboratory technician in a white coat and gloves analysing data on a computer at the Ferrer company's facilities.

During the design and execution of studies, we maintain a firm commitment to the ethical principles of clinical research, ensuring the protection of the rights, safety and well-being of participants, as well as the quality and integrity of the data generated. All trials are carried out in accordance with international ethical standards and the applicable regulations in each country.

 

In addition, we promote a collaborative approach in all phases of clinical research, working together with the scientific community, researchers, organizations and patient representatives to strengthen the design, quality and scope of our studies, always keeping the focus on the people who participate in them.

CLINICAL TRIALS AND STUDIES

  • FNP-253-CT-2502 PRECISE-HD

    Neuro

    A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Pridopidine in Participants with Huntington's Disease.

    Ongoing
  • FNP-253-CT-2503 POLSS

    Neuro

    Phase 2/3, open-label study to evaluate the safety of pridopidine in participants with Huntington's disease.

    Ongoing
  • FNP-254-CT-2501 PREVAiLS

    Neuro

    A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Pridopidine in Patients With Amyotrophic Lateral Sclerosis .

    Ongoing
  • FNP223- CT-2301 PROSPER

    Neuro

    A randomized, double-blind, placebo-controlled study to evaluate the safety, efficacy, and pharmacokinetics of FNP-223 (oral formulation) for the treatment of progressive supranuclear palsy (PSP).

    Ongoing
  • FTRI-NIS-2201

    Cardiovascular

    Multinational registry of patients in secondary cardiovascular prevention.

    Completed
  • FITREP- NIS-2401

    Respiratory

    Real-life comparative effectiveness study of Tyvaso® (inhaled treprostinil ) in the treatment of pulmonary hypertension associated with interstitial lung disease: an external comparative study of inhaled treprostinil versus standard treatment in Europe.

    Completed
  • FITREP- NIS-2402

    Respiratory

    Efficacy of inhaled treprostinil versus standard of care for the treatment of pulmonary hypertension associated with interstitial lung disease: a propensity score-weighted study from the INCREASE trial and registry data from Europe.

    Ongoing
  • FITREP- EAP-2201

    Respiratory

    Expanded access program and real-life data collection using inhaled treprostinil for the treatment of adults with pulmonary hypertension associated with interstitial lung disease.

    Ongoing
  • NEPHY

    Respiratory

    A non-interventional, retrospective, prospective study to collect data on the use, safety, and efficacy of parenteral treprostinil in neonates with pulmonary hypertension.

    Ongoing

*This table includes clinical trials of both approved products and investigational compounds. Investigational products have not been authorized for any use by the European Medicines Agency (EMA), the U.S. Food and Drug Administration (FDA), or any other health authority. The safety and efficacy of these investigational products have not been established.

Update date: July 2026