A phase 2/3 multi-center randomized, double-blind, parallel arm, placebo- controlled study in Adult Subjects Hospitalized with Severe SARS-CoV-2 Positive Pneumonia to determine the potential of opaganib to improve and/or stabilize the clinical status of the patient.
This is a phase 2/3 multi-center randomized, double-blind, parallel arm, placebo- controlled study with an adaptive design that will utilize a futility assessment. The study is planned be performed worldwide in up to approximately 80 clinical sites. After informed consent is obtained, patients will enter a screening phase for no more than 3 days, to determine eligibility. Approximately 464 eligible patients will be randomized and receive either opaganib added to standard of care, or matching placebo added to standard of care, in a randomization ratio of 1:1. Treatment assignments will remain blinded to the patient, investigator and hospital staff, as well as the sponsor. As the approval and/or guidance for treating COVID-19 are evolving, for this protocol, standard of care will be defined by the recommended schemes of treatment according to the severity of the disease, taking into consideration regulatory approvals in one or more regions. Study participants will receive either opaganib 2 x 250 mg capsules (500 mg) every 12 hours, or matching placebo, in addition to standard of care (pharmacological as defined above and/or supportive) at any given institution. Study drug will be administered every day for 14 days (Day 1 to Day 14). All participants will be followed up for 28 days after their last dose of study drug, which may occur at Day 14 or after premature study drug discontinuation, based upon patient or physician determination.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
475
Study participants will receive either opaganib 2 x 250 mg capsules (500 mg) every 12 hours, or matching placebo, in addition to standard of care (pharmacological as defined above and/or supportive) at any given institution. Study drug will be administered every day for 14 days (Day 1 to Day 14).
Study participants will receive either opaganib 2 x 250 mg capsules (500 mg) every 12 hours, or matching placebo, in addition to standard of care (pharmacological as defined above and/or supportive) at any given institution. Study drug will be administered every day for 14 days (Day 1 to Day 14).
Supplemental Oxygen Requirement
To compare the proportion of patients no longer requiring supplemental oxygen for at least 24 hours by Day 14 between subjects taking opaganib and those on placebo.
Time frame: 14 days maintained up to 42 days
Percentage of Subjects With ≥ 2 Category Improvement on the World Health Organization (WHO) Ordinal Scale for Clinical Improvement by Day 14 Maintained to Day 42
Compare ≥2 category improvement on the WHO Ordinal Scale for Clinical Improvement from 0(uninfected) to 8(death) for subjects taking opaganib and those on placebo, lower scores indicate improvement. Success was defined as subject who reached improvement of at least two points on the WHO Ordinal Scale by Day 14, maintained by the end of study visit, and failure otherwise.
Time frame: 14 days maintained up to 42 days
Number of Subjects With Improvement to a Score of 3 or Less on the WHO Ordinal Scale for Clinical Improvement With a Scale Ranging From 8 Down to 0
Compare scores of subjects taking opaganib and those on placebo, lower scores indicate improvement to determine time to recovery as defined by improvement to a score of 3 or less on the WHO Ordinal Scale for Clinical Improvement with a scale ranging from 0 (uninfected) to 8 (death)
Time frame: 14 days maintained up to 42 days
Number of Participants With Low Oxygen Flow Via Nasal Cannula
To compare the time to low oxygen flow via nasal cannula e.g. from high oxygen flow via nasal cannula or CPAP, if high oxygen flow is not an available option between subjects taking opaganib and those on placebo.
Time frame: 14 days maintained up to 42 days
Time to Discharge From Hospital Measured at 14 Days
Time to subject discharge from hospital
Time frame: 14 days
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ABC-201 Site 901
Detroit, Michigan, United States
ABC-201 Site 408
Belo Horizonte, Brazil
ABC-201 Site 411
Belo Horizonte, Brazil
ABC-201 Site 405
Joinville, Brazil
ABC-201 Site 404
Paraná, Brazil
ABC-201 Site 410
Passo Fundo, Brazil
ABC-201 Site 409
Porto Alegre, Brazil
ABC-201 Site 402
São Bernardo do Campo, Brazil
ABC-201 Site 401
São Paulo, Brazil
ABC-201 Site 403
São Paulo, Brazil
...and 47 more locations
Patients Requiring Intubation and Mechanical Ventilation by Day 42
To compare the proportion of patients requiring intubation and mechanical ventilation between subjects taking opaganib and those on placebo.
Time frame: 42 days
Number of Patients With Two Consecutive Negative Swabs for SARS-CoV-2 at Day 14
To compare the number of patients with two consecutive negative swabs for SARS-CoV-2 by PCR at Day 14 between subjects taking opaganib and those on placebo.
Time frame: 14 days
Patients With Negative Swabs for SARS-CoV-2 at Day 14
To compare the proportion of patients with two consecutive negative swabs for SARS-CoV-2 by PCR at Day 14 between subjects taking opaganib and those on placebo.
Time frame: 14 days
Mortality Due to Any Cause
To compare mortality 28 days post-baseline between subjects taking opaganib and those taking placebo
Time frame: 28 days
Mortality Due to Any Cause
To compare mortality 42 days post-baseline between subjects taking opaganib and those taking placebo
Time frame: 42 days