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Trial record 2 of 2 for:    Atr-002

Clinical Trial to Evaluate the Safety and Efficacy of ATR-002 in Adult Hospitalized Patients With COVID-19 (RESPIRE)

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ClinicalTrials.gov Identifier: NCT04776044
Recruitment Status : Recruiting
First Posted : March 1, 2021
Last Update Posted : March 16, 2021
Sponsor:
Information provided by (Responsible Party):
Atriva Therapeutics GmbH

Brief Summary:
The purpose of the study is to assess the safety and efficacy of ATR-002 (in addition to standard-of-care) for the treatment of COVID-19

Condition or disease Intervention/treatment Phase
COVID-19 Drug: ATR-002 Drug: Placebo Phase 2

Detailed Description:
After being informed about the study and potential risks, all patients giving written informed consent will be undergoing a 1-day screening to determine eligibility for study entry. At day 1, patients who meet the eligibility requirements will be randomized in a double-blind manner (participant and investigator) in a 1:1 ratio to ATR-002 (900mg day 1, 600mg days 2 - 6) or placebo (once daily)

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 220 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Intervention Model Description: Randomized, double-blind, placebo-controlled, multi-centre
Masking: Double (Participant, Investigator)
Masking Description: matching placebo tablets
Primary Purpose: Treatment
Official Title: RESPIRE - A Randomized, Double-Blind, Placebo-Controlled, Multi-Centre Clinical Trial to Evaluate the Safety and Efficacy of ATR-002 in Adult Hospitalized Patients With COVID-19
Estimated Study Start Date : March 2021
Estimated Primary Completion Date : December 2021
Estimated Study Completion Date : March 2022

Arm Intervention/treatment
Experimental: ATR-002
Participants will receive 900mg ATR-002 on day 1 (6 tablets with 150mg ATR-002; once daily), and 600mg ATR-002 on days 2 - 6 (4 tablets; once daily)
Drug: ATR-002
150mg tablets for oral intake

Placebo Comparator: Placebo
Participants will receive matching tablets placebo on day 1 (6 tablets, once daily), and matching tablets placebo on days 2 - 6 (4 tablets per day, once daily)
Drug: Placebo
matching tablets for oral intake




Primary Outcome Measures :
  1. Clinical severity status on a 7-point ordinal scale [ Time Frame: 15 days ]
    1. Not hospitalized, no limitations of activities
    2. Not hospitalized, limitations of activities
    3. Hospitalized, not requiring supplemental oxygen
    4. Hospitalized, requiring supplemental oxygen
    5. Hospitalized, on non-invasive ventilation or high flow oxygen devices
    6. Hospitalized, on invasive mechanical ventilation or ECMO
    7. Death


Secondary Outcome Measures :
  1. Time from randomization to discharge from hospital [ Time Frame: 90 days ]
  2. Time to discharge from hospital or to score of ≤2 maintained for 24 hours in NEWS2, whichever occurs first [ Time Frame: 90 days ]
  3. Time to resolution of fever, defined as ≤36.6°C (axilla), ≤37.2°C (oral) or ≤37.8°C (rectal or tympanic) for at least 24 hours without antipyretics for 24 hours [ Time Frame: 90 days ]
  4. Time to SpO2 >94% on room air maintained for 24 hours [ Time Frame: 90 days ]
  5. Clinical severity status over the hospital period calculated as AUC from the 7-point ordinal scale at Days 3, 5, 8, 11, 15 and 30 [ Time Frame: at days 3, 5, 8, 11 and 30 ]


Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. Capable of giving signed informed consent, which includes compliance with the requirements and restrictions listed in the informed consent form (ICF) and in this protocol.
  2. Study participant must be at least 18 years of age at the time of signing the ICF
  3. Study participants with a laboratory confirmed diagnosis of SARS-CoV-2 infection presenting as moderate -to-severe COVID-19 requiring hospitalization for COVID-19 (Clinical Severity Status [3] or [4]) and for medical reasons (see Section 8). Patients presenting to the hospital without a laboratory confirmed SARS-CoV-2 infection will be tested locally for SARS-CoV-2 during the screening period. For sites in the EU: A CE certified SARS-CoV-2 PCR test kit is required to confirm infection. For sites outside the EU: SARS-CoV-2 PCR test kits certified according to local regulations are required to confirm infection.
  4. Body weight at least 50 kg and a body mass index (BMI) ≥ 18.0 kg/m2 and < 40.0 kg/m2
  5. Male or female Contraceptive use by women and men should be consistent with local regulations regarding the methods of contraception for those participating in clinical studies.
  6. A female study participant is eligible to participate if she is not pregnant or breastfeeding, and one of the following conditions applies:

    1. She is not a WOCBP
    2. Is a WOCBP and is using a contraceptive method that is highly effective, with a failure rate of <1%, during the IMP period and for at least 4 weeks after the last dose of IMP. The investigator should evaluate the potential for contraceptive method failure (e.g., noncompliance, recently initiated) in relationship to the first dose of IMP.
  7. A WOCBP must have a negative urine pregnancy test within 24 hours before the first dose of IMP.

    1. If a urine pregnancy test cannot be confirmed as negative (e.g., an ambiguous result), a serum pregnancy test is required locally. In such cases, the participant must not be randomized if the serum pregnancy result is positive.
    2. If a serum pregnancy test is required as per local regulations, a serum pregnancy test is required locally. In such cases, the participant must not be randomized if the serum pregnancy result is positive.
    3. The investigator is responsible for review of medical history, menstrual history, and recent sexual activity to decrease the risk for inclusion of a woman with an early undetectable pregnancy.
  8. A male study participant is eligible to participate if:

    1. He is azoospermic
    2. The partner is not a WOCBP.
    3. The partner is a WOCBP and is using a contraceptive method that is highly effective, with a failure rate of <1%, during the IMP period and for at least 90 days after the last dose of IMP. The investigator should evaluate the potential for contraceptive method failure (e.g., noncompliance, recently initiated) in relationship to the first dose of IMP.
    4. He acknowledges that sperm donation is prohibited from the first dose of IMP until at least 90 days after the last dose of IMP.

Exclusion Criteria:

  1. Patient's clinical condition is worsening rapidly.
  2. Requiring ICU admission or ventilator support at screening or at randomization.
  3. Suspected bacterial, fungal, viral, or other infection (besides COVID-19).
  4. History of any of the following: malignant disease, autoimmune disease, or severe liver, kidney, blood, cardiac, pulmonary, neurological, or endocrine disease as judged by the investigator.
  5. History of hypertension should have hypertension adequately controlled (BP < 140/90 mmHg) with appropriate anti-hypertensive treatment.
  6. Clinically significant cardiac conduction abnormalities, including QTc prolongation of > 450 milliseconds
  7. Family history of Long QT Syndrome.
  8. Heart failure class 3, or 4, as defined by the New York Heart Association (NYHA).
  9. History of acute coronary syndrome (including myocardial infarction), coronary angioplasty, or stenting within 24 weeks prior to screening.
  10. Patients with implanted defibrillators or permanent pacemakers.
  11. Poorly controlled diabetes mellitus with an HbA1c > 7.5 %.
  12. Renal disease including glomerulonephritis, nephritic syndrome, Fanconi Syndrome, or renal tubular acidosis.
  13. Renal failure requiring renal replacement therapy or moderate renal impairment as defined by having an estimated glomerular filtration rate (eGFR, CKD-EPI) < 45 ml/min/1.73m2.
  14. Chronic Obstructive Pulmonary Disease (COPD) GOLD C, or D, or hospitalization for exacerbation of COPD within 24 weeks prior to screening.
  15. Other chronic lung diseases including cystic fibrosis, neuromuscular diseases, severe chest wall deformities, interstitial lung diseases, outpatient chronic non-invasive ventilation due to chronic respiratory failure.
  16. Asthma with a symptom control level of "uncontrolled", according to current GINA guidelines.
  17. Currently suffering from diseases that seriously affect the immune system, such as: human immunodeficiency virus (HIV) infection, or the blood system, or splenectomy, or organ/ stem cell transplantation.
  18. Known Hepatitis B or C infection.
  19. Any medical condition, physical examination finding or laboratory abnormality that, in the opinion of the investigator, might confound the results of the study or pose an additional risk to the patient.
  20. Alanine transaminase (ALT) or aspartate transaminase (AST) >3.0 x ULN.
  21. Total bilirubin >1.0 x ULN (≥1.5 x ULN total bilirubin if known Gilbert's syndrome).
  22. Taking concomitant medication metabolized by CYP2C8 and/ or CYP2C9.
  23. Taking concomitant medication of any experimental treatment or use of marketed medications including off-label use, that are intended as specific treatment for COVID-19. Any such treatments must be washed out for 30 days or at least 5 half-lives prior to randomization, whichever is longer, unless a formal written standard of care policy document requires otherwise. Inclusion needs to be approved by the investigator and medical monitor.
  24. Taking medication that may seriously affect the immune system, e.g., chemotherapy, unless considered and documented as standard of care (e.g., corticosteroids) to treat COVID-19.
  25. Currently participating in other clinical trials or previous treatment with an investigational medicinal product within 5 half-lives or 30 days (whichever is longer) prior to randomization.
  26. Known allergy or hypersensitivity to the IMP (including excipients).
  27. Study participant is pregnant or breastfeeding.
  28. Patient has been committed to an institution by virtue of an order issued either by the judicial or the administrative authorities.
  29. Patient is an employee of the sponsor, or an employee of any third-party organization involved into the clinical trial, or an employee of the clinical trial site, or is dependent on the investigator.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04776044


Contacts
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Contact: Clinical Project Management Atriva Therapeutics +49 7071 859 7673 clinicaltrials@atriva-therapeutics.com

Locations
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Sponsors and Collaborators
Atriva Therapeutics GmbH
Investigators
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Principal Investigator: University Clinic Frankfurt M Medical Clinic Centre of Pneumology
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Responsible Party: Atriva Therapeutics GmbH
ClinicalTrials.gov Identifier: NCT04776044    
Other Study ID Numbers: ATR-002-202
First Posted: March 1, 2021    Key Record Dates
Last Update Posted: March 16, 2021
Last Verified: March 2021

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No