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Trial record 4 of 688 for:    ABP 501

Study of Adalimumab or Placebo in Patients With Mild to Moderate COVID-19 (COMBAAT) (COMBAAT)

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ClinicalTrials.gov Identifier: NCT04705844
Recruitment Status : Not yet recruiting
First Posted : January 12, 2021
Last Update Posted : March 24, 2021
Sponsor:
Collaborators:
Pharm-Olam, LLC
Chemical, Biological, Radiological, and Nuclear Medical
Information provided by (Responsible Party):
Ology Bioservices

Brief Summary:
Clinical study of Humira (adalimumab) or placebo in subjects with mild-moderate COVID-19

Condition or disease Intervention/treatment Phase
Mild to Moderate COVID-19 Drug: Adalimumab Drug: Placebo Phase 3

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 1444 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Intervention Model Description: Subjects will be randomized to receive a single dose of adalimumab or placebo. Subjects will receive standard care of therapy (per study site written policies or guidelines) together with adalimumab or matching placebo.
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Masking Description: Randomized, Double-Blind, Placebo-Controlled
Primary Purpose: Treatment
Official Title: Multi-Center, Randomized, Double-Blind, Placebo-Controlled Study of Adalimumab (Humira) or Placebo in Patients With Mild-Moderate COVID-19
Estimated Study Start Date : May 2021
Estimated Primary Completion Date : November 2021
Estimated Study Completion Date : January 2022

Resource links provided by the National Library of Medicine

Drug Information available for: Adalimumab

Arm Intervention/treatment
Experimental: Adalimumab
single dose of adalimumab(160 mg administered as 4×40 mg subcutaneous [SC] injections at separate sites on the thigh or abdomen
Drug: Adalimumab
adalimumab (160 mg administered as 4×40 mg subcutaneous [SC] injections at separate sites on the thigh or abdomen)
Other Name: Humira

Placebo Comparator: Placebo
single dose of placebo (administered as 4×40 mg subcutaneous [SC] injections at separate sites on the thigh or abdomen
Drug: Placebo
placebo (4 SC injections of equal volume administered at separate sites on the thigh or abdomen)




Primary Outcome Measures :
  1. Establish whether treatment with adalimumab is associated with a lower rate of progression to severe disease as defined by severe illness or critical illness, or death in outpatient subjects with COVID-19 [ Time Frame: 28 Days ]

    Proportion of subjects with the following outcomes attributed to COVID-19 from time of first dose through Day 28 following randomization:

    • Death
    • Alive and hospitalized or requiring supplemental oxygen for ≥1 hour
    • Alive and not hospitalized or requiring supplemental oxygen for ≥1 hour

  2. Assess the safety of adalimumab in subjects with COVID-19 [ Time Frame: 28 Days ]
    Incidence of Grade 3 and Grade 4 clinical adverse events (AEs) from first dose through Day 28 following randomization


Secondary Outcome Measures :
  1. Assess the impact of treatment with adalimumab on clinical course of COVID-19 infection [ Time Frame: 120 Days ]

    Clinical status by 9-point WHO COVID 19 ordinal scale from first dose through Day 120 following randomization

    • Incidence of venous thromboembolism, CVA, myocardial infarction, and acute kidney injury C from first dose through Day 120 following randomization
    • Time to resolution of symptoms using 14 point COVID-19 Symptom Score from first dose through Day 120 following randomization
    • COVID-19 Clinical Assessment from first dose through Day 120 following randomization



Information from the National Library of Medicine

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Ages Eligible for Study:   40 Years to 80 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Subject (or their legally authorized representative) is willing and able to provide written informed consent prior to performing study procedures.
  • Understands and agrees to comply with planned study procedures.
  • Male or non-pregnant female adult ≥60 and ≤ 80years of age OR male or non-pregnant female adult ≥40 and ≤80 years, with one or more of the following risk factors (asthma, diabetes, hypertension, obesity [body mass index >30], cardiovascular disease).
  • Has a laboratory-confirmed SARS-CoV-2 infection as determined by FDA-approved rapid diagnostic (e.g., polymerase chain reaction [PCR]) assay within the preceding 7 days (168 hours).
  • Has at least 2 COVID-19 related symptoms on the 14-question COVID-19 questionnaire.
  • Has peripheral capillary oxygen saturation (SpO2) >93% by pulse oximetry.
  • C-reactive protein (CRP) >50 mg/L or lymphopenia (<1.5×109/L) or neutrophilia (>7.5×109/L).
  • Agrees to the collection of blood and urine samples, nasal swabs , and non-invasive oxygen monitoring (via pulse oximeter) per protocol.
  • Willing to receive 4 injections at separate sites on the thigh or abdomen.
  • Women of childbearing potential must agree to either abstinence or use of at least one primary form of contraception (not including hormonal contraception) from the time of screening through Day 29 following randomization.
  • Agrees to not participate in any other clinical trial (both pharmacologic and other types of interventions) through Day 29 following randomization

Exclusion Criteria:

  • Received or contemplating any COVID-19 vaccine or participated in a COVID-19 vaccine trial.
  • Subject is considered to be in their last few weeks of life prior to this acute illness.
  • History of pulmonary alveolar proteinosis.
  • History of hematopoietic stem cell transplant or solid organ transplant.
  • Previous malignancy and lymphoproliferative disorders (within the last 5 years) with the exception of stable prostate cancer and basal cell carcinoma.
  • Chronic obstructive pulmonary disease on long-term oxygen therapy - subjects with forced expiratory volume in 1 second known to be <50% will also be excluded.
  • Demyelinating disease.
  • Known history of hepatitis B, HIV, or untreated hepatitis C infection
  • Severe hepatic impairment or known cirrhosis - Child-Pugh score B or higher.
  • Acute kidney injury Stage 3
  • Tuberculosis or other severe infections such as (non-COVID-19) sepsis, abscesses, fungal superinfection and opportunistic infections requiring treatment.
  • Positive Quantiferon Gold test at screening
  • Moderate or severe heart failure (New York Heart Association Class III/IV).
  • Treatment with monoclonal antibodies targeting cytokines (e.g., TNF inhibitors [adalimumab, infliximab, etanercept, golimumab, certolizumab]; anti-IL-1 [e.g., anakinra, canakinumab]; anti-IL-6 or anti-IL-6r [e.g., tocilizumab, sarilumab, sitlukimab]; or T-cells [e.g., abatacept]) in past 90 days (5 half-lives of the drug), or contemplating treatment with any of these agents during the trial period.
  • Treatment with monoclonal antibodies targeting B-cells (e.g., rituximab, and including any targeting multiple cell lines including B-cells) in the 3 months prior to screening.
  • Received GM-CSF agents (e.g., sargramostim) within 2 months prior to screening.
  • Treatment with other immunosuppressants in the 4 weeks prior to screening and in the judgment of the Investigator, the risk of immunosuppression with adalimumab is larger than the risk of COVID-19.
  • Treatment with small molecule tyrosine kinase inhibitors (e.g., baricitinib, ibrutinib, acalabrutinib, imatinib, gefitinib), in the 4 weeks prior to screening.
  • Received or contemplating receipt of any live vaccine or any investigational vaccine in the 4 weeks prior to screening.
  • Current participation or previous participation in any other clinical trial within 30 days prior to randomization.
  • Subjects with known hypersensitivity to adalimumab or excipients of adalimumab as stated in the label.
  • Pregnant female
  • Lactating female
  • Women of childbearing potential who do not agree to either abstinence or use of at least one primary form of contraception (not including hormonal contraception) from the time of screening through Day 29 following randomization.
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Responsible Party: Ology Bioservices
ClinicalTrials.gov Identifier: NCT04705844    
Other Study ID Numbers: A21-070
First Posted: January 12, 2021    Key Record Dates
Last Update Posted: March 24, 2021
Last Verified: March 2021
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Adalimumab
Anti-Inflammatory Agents
Antirheumatic Agents