Details of Umifenovir
Name of trial | Phase III, Randomized, Double-blind, Placebo controlled trial of Efficacy, Safety and Tolerability of Antiviral drug Umifenovir vs Standard care of therapy in non-severe COVID-19 patients. | |||||||
CSIR lab/s involved | Industry Sponsor/s & Scientific Collaborator/s | Clinical Trial Site/s | ||||||
CSIR-CDRI
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M/s Medizest Pharmaceuticals Pvt Ltd. | King George’s Medical University, Ram Manohar Lohia Institute of Medical Sciences, Eras Lucknow Medical College and Hospital, Lucknow |
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Type of Drug | Antiviral | |||||||
IP Status of Drug/s |
Out of IP | |||||||
Mechanism of Action & Scientific rationale for Covid-19 |
1. Broad spectrum antiviral agent 2. Prevents viral entry into human host cells 3. Host targeting agent |
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Combinations therapy or monotherapy | Combination therapy with ‘Standard of care’ | |||||||
Trial design |
Health Condition / Problems Studied |
Health Type | Condition | |||||
COVID19 patients | Mild and moderate symptoms |
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Click here for End points (primary and secondary) |
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Status of the CSIR trial |
Patient recruitment has been initiated |
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Name & details of Clinical PI/s | Dr. VirendraAtam, KGMU, Lucknow, Dr. Vikram Singh, RMLIMS, Lucknow, Dr. MMA Faridi, Eras Medical College, Lucknow, Dr. Vivek Bhosale, CSIR-CDRI, | Administrative PI and Nodal scientist: Dr. R. Ravishankar, CSIR-CDRI, Lucknow Prof. Tapas K. Kundu, Director, CSIR-CDRI |
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