Efficacy and Safety Study of OATD-01 in Patients With Active Pulmonary Sarcoidosis

Recruiting now · Phase 2 · Has a placebo group

Conditions studied: Pulmonary Sarcoidosis

In brief

This is a Phase 2, randomized, double-blind, placebo-controlled, adaptive, multicenter study to evaluate the efficacy, safety, tolerability, Pharmacodynamics (PD), and Pharmacokinetics (PK) of OATD-01 in the treatment of subjects with active pulmonary sarcoidosis.

Key facts

Study ID

NCT06205121

Run by

Molecure S.A.

People needed

96

Starts

2024-03-21

Expected to finish

2027-09-01

Last updated by the study team

2026-07-30

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Male and female subjects with active symptomatic pulmonary sarcoidosis, (definite diagnosis of active pulmonary sarcoidosis per ATS guidelines)
• Treatment-naïve or previously treated (no recruitment cap)
• Parenchymal pulmonary involvement on [18F]FDG PET/CT

You may not qualify if…

• Requirement for immediate start of standard of care therapy for pulmonary sarcoidosis
• Active cardiac or neuro- sarcoidosis
• History of/active Löfgren syndrome
• Clinically significant lung disease other than sarcoidosis (e.g. tuberculosis, asthma, Chronic Obstructive Pulmonary Disease, interstitial lung disease, lung cancer) or any current inflammatory or immunological systemic disease other than sarcoidosis
• Potentially effective systemic or inhaled pharmacological (including investigational) therapy for sarcoidosis (whether pulmonary or other disease), with the exception of any of the following:
• corticosteroids received not later than 3 months prior to enrolment
• immunosuppressants or anti-Tumor Necrosis Factor (TNF) agents (or other anti-inflammatory/anti-fibrotic treatment) received not later than 4 months prior to enrolment
• Systemic treatment indication being an extrapulmonary location of sarcoidosis (e.g., neurological)
• Heart conditions: QTcF interval prolongation, cardiac arrhythmia (other than non-sustained supraventricular arrhythmia), heart failure (New York Heart Association class III or IV) and/or known myocardial hypertrophy or Left Ventricle Ejection Fraction \<50% in the cardiac MRI
• Known neurosarcoidosis or small fiber neuropathy or medical conditions causing primary ataxia
• Lab abnormalities: Abnormal bilirubin, transaminases, alkaline phosphatase (ALP), Creatinine clearance (CrCL) Hypokalemia hypocalcemia (\<2.1 mmol/L), marked fasting hyperglycemia at screening
• Uncontrolled diabetes at Screening with plasma glucose exceeding 8.3 mmol/L, or other contraindication to [18F]FDG administration and/or PET procedure (including body temperature \>37°C and any metabolic disease affecting the energy metabolism of muscles) as described in the PET protocol
• Known positivity for Human Immunodeficiency Virus (HIV 1/2 antibodies), hepatitis B virus (HBV), or hepatitis C virus (HCV), or detected at screening
• Severe, uncontrolled systemic disease (e.g., cardiovascular, pulmonary, thyroid, renal or metabolic disease) at Screening, or other condition, which in the opinion of the investigator, would compromise the safety of the subject or the subject's ability to participate in the study
• Current smoker of \>5 cigarettes or e-cigarettes per day or user of nicotine-releasing alternatives (patches, chewing gums etc)
• Prohibited medications: Current treatment with drug with QT prolongation effect, thiazide diuretics, strong CYP3A4 inhibitors and/or inducers, P-glycoprotein and/or BCRP strong inhibitors, drugs that are sensitive substrates of OCT1, MATE1, MATE2K, OAT3 with a narrow therapeutic index, pirfenidone and nintedanib.

Where it is running

• Molecure Investigative Site — London, United Kingdom (enrolling)
• Molecure Investigative Site — Nieuwegein, Netherlands (enrolling)
• Molecure Investigative Site — Rotterdam, Netherlands (enrolling)
• Molecure Investigative Site — Bergen, Norway (enrolling)
• Molecure Investigative Site — Oslo, Norway (enrolling)
• Molecure Investigative Site — Birmingham, United Kingdom (enrolling)
• Molecure Investigative Site — Edinburgh, United Kingdom (enrolling)
• Molecure Investigative Site — London, United Kingdom (enrolling)
• Molecure Investigative Site — Baltimore, Maryland, United States (enrolling)
• Molecure Investigative Site — Cleveland, Ohio, United States (enrolling)
• Molecure Investigative Site — Philadelphia, Pennsylvania, United States (enrolling)
• Molecure Investigative Site — Charleston, South Carolina, United States (enrolling)
• Molecure Investigative Site — Montpellier, France (enrolling)
• Molecure Investigative Site — Paris, France (enrolling)
• Molecure Investigative Site — Paris, France (enrolling)
• Molecure Investigative Site — Essen, Germany (enrolling)
• Molecure Investigative Site — Freiburg im Breisgau, Germany (enrolling)
• Molecure Investigative Site — Mainz-GE, Germany (enrolling)
• Molecure Investigative Site — Heraklion, Greece (enrolling)
• Molecure Investigative Site — Pátrai, Greece (enrolling)
• Molecure Investigative Site — Thessaloniki, Greece (enrolling)
• Molecure Investigative Site — Kansas City, Kansas, United States
• Molecure Investigative Site — Bobigny, France
• Molecure Investigative Site — Rochester, Minnesota, United States
• Molecure Investigative Site — Corfu, Greece

Full record on ClinicalTrials.gov

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