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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04939428
Other study ID # 4482-013
Secondary ID MK-4482-013jRCT2
Status Completed
Phase Phase 3
First received
Last updated
Start date August 11, 2021
Est. completion date November 16, 2022

Study information

Verified date January 2024
Source Merck Sharp & Dohme LLC
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of the study is to assess if the study medication (molnupiravir, MK-4482) will prevent symptomatic coronavirus disease 2019 (COVID-19) in adults who live with someone with confirmed COVID-19 infection. This is a phase 3, multicenter, randomized, double-blind, placebo-controlled study; half of the study participants will receive molnupiravir twice daily by mouth and the other half will receive a placebo. The primary objectives of the study are to determine if molnupiravir prevents symptomatic COVID-19 disease and to evaluate its safety and tolerability. All participants who develop COVID-19 during the study are still eligible for any COVID-19 treatment recommended by their doctor.


Recruitment information / eligibility

Status Completed
Enrollment 2441
Est. completion date November 16, 2022
Est. primary completion date November 16, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Lives in a household with an index case where the index case is a person with documented COVID-19 (laboratory-confirmed SARS-CoV-2 infection with symptoms case) and must have 1) a first detectable SARS-CoV-2 test result from a sample collected within =5 days prior to randomization of the participant, and 2) at least 1 symptom attributable to COVID-19 (e.g., fever, difficulty breathing) - Does not have confirmed or suspected COVID-19 - Is willing and able to take oral medication - For males, agrees to be abstinent from penile-vaginal intercourse OR agrees to use a highly effective contraceptive method while receiving study drug and for =3 months after the last dose of study drug - Is female and not pregnant/breastfeeding and at least one of the following applies during the study and for =4 days after: is not a woman of childbearing potential (WOCBP), is a WOCBP and uses highly effective contraception (low user dependency method OR a user dependent hormonal method in combination with a barrier method), or is a WOCBP who is abstinent from heterosexual intercourse Exclusion Criteria: - Has a prior history of laboratory-confirmed SARS-CoV-2 infection (with or without symptoms) within 6 months prior to randomization - Has either of the following: human immunodeficiency virus (HIV) with a recent viral load >50 copies/mL (regardless of CD4 count) or an acquired immunodeficiency syndrome (AIDS)-defining illness - Has a history of hepatitis B virus (HBV) or hepatitis C virus (HCV) infection with any of the following: cirrhosis, end-stage liver disease, hepatocellular carcinoma; aspartate transaminase (AST) and/or (ALT) >3x upper limit of normal at screening - Has hypersensitivity or other contraindication to any of the components of the study interventions as determined by the investigator - Has any condition for which, in the opinion of the investigator, participation would not be in the best interest of the participant or that could prevent, limit, or confound the protocol-specified assessments including but not limited to participants with conditions that could limit gastrointestinal absorption of capsule contents - Has received, is taking, or is anticipated to require any prohibited therapies - Has received a COVID-19 vaccination with the first dose =7 days prior to randomization - Is unwilling to abstain from participating in another interventional clinical study through Day 29 with an investigational compound or device, including those for COVID-19 therapeutics - Is living in a household with >10 people

Study Design


Intervention

Drug:
Molnupiravir
Four molnupiravir 200 mg capsules taken by mouth.
Placebo
Placebo capsule matched to molnupiravir 200 mg capsules taken by mouth.

Locations

Country Name City State
Argentina CEMIC ( Site 0101) Buenos Aires
Argentina Hospital Italiano de Buenos Aires ( Site 0102) Caba Buenos Aires
Argentina Mautalen Salud e Investigacion ( Site 0103) Caba Buenos Aires
Argentina Sanatorio de la Trinidad Mitre ( Site 0108) Caba Buenos Aires
Argentina Instituto de Investigaciones Clínicas Mar del Plata ( Site 0105) Mar del Plata Buenos Aires
Argentina Clinica Independencia ( Site 0104) Munro Buenos Aires
Argentina Instituto Medico de la Fundacion Estudios Clinicos ( Site 0106) Rosario Santa Fe
Argentina Grupo Oroño Centro medico San Nicolas ( Site 0109) San Nicolas Buenos Aires
Brazil Faculdade de Medicina da Universidade Federal de Mato Grosso do Sul - UFMS ( Site 0305) Campo Grande Mato Grosso Do Sul
Brazil Hospital Nossa Senhora das Gracas ( Site 0310) Curitiba Parana
Brazil Oncosite-Centro de Pesquisa Clinica em Oncologia ( Site 0300) Ijui Rio Grande Do Sul
Brazil Fundaçao de Medicina Tropical Doutor Heitor Vieira Dourado ( Site 0303) Manaus Amazonas
Brazil Centro de Referencia Professor Helio Fraga - FIOCRUZ/RJ ( Site 0314) Rio de Janeiro
Brazil Fundação Faculdade Regional de Medicina de São José do Rio Preto ( Site 0312) São José do Rio Preto Sao Paulo
Brazil Centro de Referência e Treinamento DST/AIDS ( Site 0301) Sao Paulo
Bulgaria Medical Center Hera Kyustendi EOOD ( Site 3003) Kyustendil
Bulgaria Medical Center Hera EOOD - Montana branch ( Site 3002) Montana
Bulgaria Medical Center Hera EOOD ( Site 3001) Sofia Sofia (stolitsa)
Colombia Centro Cientifico Asistencial Jose Luis Accini ( Site 0412) Barranquilla Atlantico
Colombia Clinica de la Costa Ltda. ( Site 0407) Barranquilla Atlantico
Colombia Caja de Compensacion Familiar CAFAM ( Site 0403) Bogota Distrito Capital De Bogota
Colombia Hospital Universitario Clinica San Rafael ( Site 0410) Bogota Cundinamarca
Colombia Instituto Neumologico del Oriente S.A. ( Site 0408) Bucaramanga Santander
Colombia Fundacion Valle del Lili ( Site 0405) Cali Valle Del Cauca
Colombia Fundacion Centro de Investigacion Clinica CIC ( Site 0402) Medellin Antioquia
Colombia Oncomedica S.A. ( Site 0406) Monteria Cordoba
Colombia Fundacion Centro de Investigaciones Clinicas CARDIOMET ( Site 0409) Pereira Risaralda
Colombia Healthy Medical Center S.A.S ( Site 0413) Zipaquira Cundinamarca
Dominican Republic Unidad de Aislamiento del Centro de Obstetricia y Ginecologia ( Site 2650) Santo Domingo Distrito Nacional
Egypt Air Force Specialized Hospital Clinical Research Center ( Site 2920) Cairo Al Qahirah
Egypt Masri - CRC - Ain Shams University ( Site 2900) Cairo Al Qahirah
Egypt Masri - CRC - Ain Shams University ( Site 2910) Cairo Al Qahirah
Egypt National Hepatology and Tropical Medicine Research Institute ( Site 2930) Cairo Al Qahirah
Egypt Imbaba Fevers Hospital ( Site 2945) Giza Al Jizah
Egypt National Center for allergies and chest ( Site 2940) Giza Al Jizah
France CHU Martinique ( Site 0511) Fort-de-France Martinique
France Maison de santé du Pays Neufchatelois ( Site 0507) Neufchatel-en-Bray Seine-Maritime
France Hôpital Pitié - Salpêtrière ( Site 0501) Paris Ile-de-France
France CHU de la Reunion - Groupe Hospitalier Sud ( Site 0508) Saint Pierre Cedex La Reunion
France Maison de Sante Universitaire La Providence ( Site 0506) Toulouse Haute-Garonne
Guatemala Centro de Investigaciones Pediatricas ( Site 0703) Guatemala
Guatemala Clínica Médica Especializada en Pediatría e Infectología Pediátrica - Dr. Mario Melgar ( Site 0702) Guatemala
Guatemala Clinica Privada ( Site 0705) Guatemala
Guatemala Private Clinic - Dr. Hugo Pezzarossi ( Site 0704) Guatemala
Guatemala Unidad de Diagnostico Cardiologico ( Site 0701) Guatemala
Hungary DRC Gyogyszervizsgalo Kozpont Kft. ( Site 0801) Balatonfured Veszprem
Hungary Obudai Egeszsegugyi Centrum - OEC ( Site 0821) Budapest
Hungary Strazsahegy Medicina Bt ( Site 0823) Budapest
Hungary Debreceni Egyetem Klinikai Kozpont- Infektologiai Klinika ( Site 0824) Debrecen Hajdu-Bihar
Hungary Bugat Pal Korhaz ( Site 0817) Gyongyos Heves
Hungary Medifarma-98 Kft. ( Site 0808) Nyiregyhaza Szabolcs-Szatmar-Bereg
Hungary LONA MEDIC Kft ( Site 0804) Oroshaza Bekes
Hungary Obudai Egeszsegugyi Centrum - Zalaegerszeg ( Site 0819) Zalaegerszeg
Japan Chiba Aoba Municipal Hospital ( Site 1100) Chiba
Japan National Hospital Organization Okinawa National Hospital ( Site 1109) Ginowan Okinawa
Japan IUHW Narita Hospital ( Site 1105) Narita Chiba
Japan Center Hospital of the National Center for Global Health and Medicine ( Site 1101) Tokyo
Japan Den-en-chofu family clinic ( Site 1104) Tokyo
Japan Global Healthcare Clinic ( Site 1106) Tokyo
Japan Sekino Hospital ( Site 1110) Tokyo
Japan Social Medical Corporation Yuuaikai Yuuai Medical Center ( Site 1108) Tomigusuku Okinawa
Kenya KEMRI-CMR-RCTP- Kenya Medical Research Institute Kisumu ( Site 1925) Kisumu
Kenya Center for Clinical Research (CCR) KEMRI ( Site 1929) Nairobi Nairobi City
Kenya Partners in Health Research and Development PHRD ( Site 1928) Nairobi Nairobi City
Malaysia Hospital Raja Perempuan Zainab II ( Site 2851) Kota Bharu Kelantan
Malaysia Klinik Kesihatan Masjid Tanah ( Site 2850) Masjid Tanah Melaka
Mexico Hospital General de Acapulco ( Site 1319) Acapulco Guerrero
Mexico Centro de Investigacion Medica Aguascalientes ( Site 1305) Aguascalientes
Mexico Centro de Investigacion y Avances Medicos Especializados -CIAME ( Site 1301) Cancun Quintana Roo
Mexico ICARO Investigaciones en Medicina ( Site 1313) Chihuahua
Mexico Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran ( Site 1308) Ciudad de Mexico Distrito Federal
Mexico Centro Médico Universitario ( Site 1316) Cuernavaca Morelos
Mexico CHRISTUS - LATAM HUB CENTER OF EXCELLENCE AND INNOVATION S.C. ( Site 1315) Gral Escobedo Nuevo Leon
Mexico Instituto Jalisciense de Metabolismo SC ( Site 1314) Guadalajara Jalisco
Mexico Morales Vargas Centro de Investigacion, S.C. ( Site 1318) Leon Guanajuato
Mexico Köhler & Milstein Research S.A. de C.V. ( Site 1300) Merida Yucatan
Mexico Medica Sur S.A.B de C.V. ( Site 1303) Mexico City
Mexico Oaxaca Site Management Organization S.C. ( Site 1304) Oaxaca
Mexico Arké SMO S.A de C.V ( Site 1306) Veracruz
Peru Policlínico Especializado en Neurología - Unid. Inv. Neurológica ( Site 1403) La Perla Qallaw
Peru Asociacion Civil IMPACTA Salud y Educacion - Sede San Miguel ( Site 1410) Lima
Peru Asociacion Civil por la Salud ( Site 1411) Lima
Peru Clinica Providencia ( Site 1400) Lima
Peru Clínica Ricardo Palma ( Site 1406) Lima
Peru Instituto de Investigacion Nutricional - Anexo Huascar ( Site 1404) Lima
Peru Investigaciones Medicas en Salud - INMENSA ( Site 1401) Lima
Philippines Health Index Multi-Specialty and Lying -in Clinic ( Site 1504) Cavite
Philippines Asian Hospital and Medical Center ( Site 1503) Muntinlupa National Capital Region
Philippines Quirino Memorial Medical Center ( Site 1501) Quezon City National Capital Region
Romania Centrul Medical Unirea ( Site 1705) Brasov
Romania Centrul Medical Unirea SRL Bucuresti ( Site 1706) Bucharest
Romania Delta Heath Care S.R.L ( Site 1708) Bucharest
Romania SC Policlinica CCBR SRL. Bucuresti ( Site 1704) Bucharest
Romania Centrul Medical Unirea SRL ( Site 1707) Cluj-Napoca Cluj
Romania Centrul Medical Unirea SRL Constanta ( Site 1703) Constanta
Romania Centrul Medical Unirea SRL IASI ( Site 1701) Iasi
Romania S.C Materna Care SRL ( Site 1702) Timisoara Timis
Russian Federation Republican Clinical Infectious Hospital n.a. A.F. Agafonov ( Site 1802) Kazan Tatarstan, Respublika
Russian Federation FSBI Central Hospital with Policlinics ( Site 1807) Moscow Moskva
Russian Federation Infectious Clinical Hospital # 1 ( Site 1834) Moscow Moskva
Russian Federation Nikolaevskaya hospital ( Site 1810) Saint Petersburg Sankt-Peterburg
Russian Federation Smorodintsev Research Institute of Influenza ( Site 1833) Saint Petersburg Sankt-Peterburg
Russian Federation SPb SBHI City outpatient clinic 112 ( Site 1829) Saint Petersburg Sankt-Peterburg
Russian Federation SPb SBHI City outpatient clinic 4 ( Site 1831) Saint Petersburg Sankt-Peterburg
Russian Federation City Polyclinic #88 ( Site 1808) Saint-Petersburg Sankt-Peterburg
Russian Federation Limited liability company "Scientific research center Eco-safety" ( Site 1809) Saint-Petersburg Sankt-Peterburg
Russian Federation LLC -Medical Center . Capital-Polis ( Site 1825) Saint-Petrsburg Sankt-Peterburg
Russian Federation St.Petersburg Outpatient Clinic No. 109 ( Site 1818) Saint-Petrsburg Sankt-Peterburg
Russian Federation Smolensk State Medical Academy ( Site 1803) Smolensk Smolenskaya Oblast
Russian Federation Medical Research Institute LLC. ( Site 1814) St.Petersburg Sankt-Peterburg
Russian Federation SPb SBHI. City outpatient clinic No.44 ( Site 1830) St.Petersburg Sankt-Peterburg
Russian Federation Voronezh Regional Clinical Hospital #1 ( Site 1823) Voronezh Voronezskaja Oblast
Russian Federation LLC -Clinic of modern medicine of Doctor Bogorodskaya ( Site 1828) Yaroslavl Yaroslavskaya Oblast
South Africa IATROS International ( Site 1921) Bloemfontein Free State
South Africa REIMED Reiger Park ( Site 1910) Boksburg Gauteng
South Africa DTHF Masiphumelele Clinical Research Site ( Site 1919) Cape Town Western Cape
South Africa TASK Applied Science ( Site 1920) Cape Town Western Cape
South Africa Dr Jugnundun & Partners ( Site 1905) Durban Kwazulu-Natal
South Africa Enhancing Care Foundation-DICRS ( Site 1922) Durban Kwazulu-Natal
South Africa Private Practice - Dr. Neyaseelan Gounden ( Site 1911) Durban Kwazulu-Natal
South Africa Midrand Medical Centre ( Site 1913) Halfway House Gauteng
South Africa Right To Care Research - Esizayo ( Site 1907) Johannesburg Gauteng
South Africa Wits Health Consortium. Clinical HIV Research Unit ( Site 1923) Johannesburg Gauteng
South Africa DJW Navorsing ( Site 1915) Krugersdorp Gauteng
South Africa Zinakekele Medical Centre ( Site 1926) Moloto Gauteng
South Africa Mzansi Ethical Research Centre ( Site 1918) Mpumalanga Gauteng
South Africa Be Part Yoluntu Centre ( Site 1914) Paarl Western Cape
South Africa Paarl Research Centre ( Site 1924) Paarl Western Cape
South Africa Global Clinical Trial Centre ( Site 1904) Pretoria Gauteng
South Africa Jongaie Research ( Site 1900) Pretoria-West Gauteng
South Africa Limpopo Clinical Research Initiative ( Site 1901) Thabazimbi Limpopo
Spain Hospital de Alcorcon ( Site 2003) Alcorcon Madrid, Comunidad De
Spain Hospital Universitari Germans Trias i Pujol ( Site 2010) Badalona Barcelona
Spain C.S. Vallcarca-Sant Gervasi ( Site 2000) Barcelona
Spain CAP de Sardenya ( Site 2009) Barcelona
Spain CAP Centelles ( Site 2011) Centelles Barcelona
Spain Hospital Universitario Infanta Leonor ( Site 2002) Madrid
Spain Hospital Universitario La Paz ( Site 2024) Madrid
Thailand HIV-NAT AIDS Research Centre ( Site 2804) Bangkok Krung Thep Maha Nakhon
Thailand Songklanagarind Hospital ( Site 2802) Hat-Yai Songkhla
Thailand Chulabhorn Hospital ( Site 2801) Lak Si Krung Thep Maha Nakhon
Thailand The Golden Jubilee Medical Center ( Site 2800) Phutthamonthon Nakhon Pathom
Thailand Rajavithi Hospital ( Site 2803) Ratchathewi Krung Thep Maha Nakhon
Turkey Ankara Sehir Hastanesi ( Site 2111) Ankara
Turkey Ankara Universitesi Ibni Sina Hastanesi ( Site 2101) Ankara
Turkey Gazi Universitesi Tip Fakultesi Hastanesi ( Site 2106) Ankara
Turkey Hacettepe Universitesi Tip Fakultesi ( Site 2102) Ankara
Turkey Atakent Acibadem Hastanesi ( Site 2103) Halkali/K.cekmece Istanbul
Turkey Basaksehir Cam ve Sakura City Hospital ( Site 2112) Istanbul
Turkey Istanbul Universitesi Istanbul Tip Fakultesi ( Site 2110) Istanbul
Turkey Medipol Universite Hastanesi ( Site 2108) Istanbul
Turkey Sancaktepe Prof Dr Ilhan Varank EAH-Prof Dr Feriha Oz Hastanesi ( Site 2113) Istanbul
Turkey Ege Universitesi Tip Fakultesi Hastanesi ( Site 2105) Izmir
Turkey Sakarya Universitesi Egitim ve Arastirma Hastanesi ( Site 2107) Sakarya
Ukraine Ivano-Frankivsk Regional Clinical Infectious Diseases Hospital ( Site 2232) Ivano-Frankivsk Ivano-Frankivska Oblast
Ukraine NPME -Central Clinical Hospital of Ivano-Frankivsk City Council ( Site 2204) Ivano-Frankivsk Ivano-Frankivska Oblast
Ukraine Regional Phthisiopulmonological Center ( Site 2203) Ivano-Frankivsk Ivano-Frankivska Oblast
Ukraine Non profit municipal enterprise City hospital student of Kharkiv city council ( Site 2229) Kharkiv Kharkivska Oblast
Ukraine PCNE Kharkiv City polyclinic 9 of the Kharkiv City Council ( Site 2201) Kharkiv Kharkivska Oblast
Ukraine Kyiv railway clinical hospital 2 of Branch Health center ( Site 2207) Kyiv Kyivska Oblast
Ukraine Limited Liability Company Medical center Healthy Happy ( Site 2225) Kyiv Kyivska Oblast
Ukraine MNPE Consultative-Diagnostic Centre of Desnyanskyi District of Kyiv ( Site 2205) Kyiv Kyivska Oblast
Ukraine Municipal Noncommercial Enterprise Lviv 4th City Clinical Hospital ( Site 2200) Lviv Lvivska Oblast
Ukraine Odesa Regional Center of Socially Significant Diseases ( Site 2230) Odesa Odeska Oblast
Ukraine MNCE -Odesa regional clinical hospital of Odesa regional council ( Site 2226) Odessa Odeska Oblast
Ukraine Municipal Enterprise Poltava Regional Clinical Infectious Hospital ( Site 2227) Poltava Poltavska Oblast
Ukraine Medical Clinical Investigational Center of Medical Center Health Clinic ( Site 2210) Vinnytsia Vinnytska Oblast
United States PharmaTex Research, LLC ( Site 2541) Amarillo Texas
United States Institute of Human Virology ( Site 2504) Baltimore Maryland
United States Cahaba Research, Inc. ( Site 2523) Birmingham Alabama
United States TTS Research ( Site 2433) Boerne Texas
United States Synergy Healthcare ( Site 2521) Bradenton Florida
United States Montefiore Medical Center ( Site 2503) Bronx New York
United States Mercury Street Medical Group PLLC ( Site 2476) Butte Montana
United States Hope Clinical Research ( Site 2400) Canoga Park California
United States Carbon Health ( Site 2515) Carlsbad California
United States Chicago Clinical Research Institute Inc ( Site 2454) Chicago Illinois
United States Rush University Medical Center ( Site 2510) Chicago Illinois
United States The Lindner Center for Research and Education at The Christ Hospital ( Site 2517) Cincinnati Ohio
United States Future Innovative Treatments, LLC ( Site 2471) Colorado Springs Colorado
United States University of Missouri Hospital ( Site 2486) Columbia Missouri
United States Dayton Clinical Research ( Site 2488) Dayton Ohio
United States Accel Research Sites-DeLand Clinical Research Unit ( Site 2535) DeLand Florida
United States Velocity Clinical Research-Providence ( Site 2432) East Greenwich Rhode Island
United States Centennial Medical Group ( Site 2435) Elkridge Maryland
United States Michigan Center of Medical Research ( Site 2445) Farmington Hills Michigan
United States Prime Health and Wellness/SKYCRNG ( Site 2538) Fayette Mississippi
United States UCSF Fresno ( Site 2528) Fresno California
United States ASCADA Research, LLC ( Site 2516) Fullerton California
United States ECU Adult Specialty Care ( Site 2415) Greenville North Carolina
United States Tribe Clinical Research, LLC ( Site 2409) Greenville South Carolina
United States Velocity Clinical Research, Hallandale Beach ( Site 2485) Hallandale Beach Florida
United States Indago Research and Health Center Inc ( Site 2412) Hialeah Florida
United States ID Care ( Site 2466) Hillsborough New Jersey
United States Houston Methodist Hospital ( Site 2463) Houston Texas
United States Santa Clara Family Clinic ( Site 2462) Houston Texas
United States Marvel Clinical Research ( Site 2490) Huntington Beach California
United States Advanced Research For Health Improvement LLC ( Site 2436) Immokalee Florida
United States Excel Clinical Research, LLC ( Site 2404) Las Vegas Nevada
United States Michigan Center of Medical Research ( Site 2525) Lathrup Village Michigan
United States Balanced Life Healthcare Solutions/SKYCRNG ( Site 2539) Lawrenceville Georgia
United States National Research Institute ( Site 2452) Los Angeles California
United States The Institute for Liver Health DBA Arizona Clinical Trials ( Site 2484) Mesa Arizona
United States MedPharmics, LLC ( Site 2443) Metairie Louisiana
United States Southern Clinical Research Associates ( Site 2542) Metairie Louisiana
United States Clinical Site Partners, LLC d/b/a CSP Miami ( Site 2508) Miami Florida
United States Allina Health Infectious Diseases Research Clinic ( Site 2507) Minneapolis Minnesota
United States Valley Clinical Trials Inc. ( Site 2406) Northridge California
United States Carbon Health ( Site 2514) Oakland California
United States University of Nebraska Medical Center ( Site 2430) Omaha Nebraska
United States Preferred Clinical Research ( Site 2470) Pittsburgh Pennsylvania
United States CDC Research Institute, LLC ( Site 2540) Port Saint Lucie Florida
United States Amici Clinical Research LLC ( Site 2426) Raritan New Jersey
United States Quinn Healthcare/Skycrng ( Site 2537) Ridgeland Mississippi
United States University of California Davis ( Site 2497) Sacramento California
United States AXCES Research Group ( Site 2437) Santa Fe New Mexico
United States Covid-19 Clinical Research Center (CCRC) ( Site 2421) Seattle Washington
United States Jadestone Clinical Research, LLC ( Site 2530) Silver Spring Maryland
United States Millennium Clinical Trials ( Site 2468) Simi Valley California
United States Cherokee Nation WW Hastings Indian Hospital/Cherokee Nation Health Services ( Site 2459) Tahlequah Oklahoma
United States Clinical Research Trials of Florida ( Site 2402) Tampa Florida
United States The Institute for Liver Health DBA Arizona Clinical Trials ( Site 2448) Tucson Arizona
United States Crossroads Clinical Research LLC ( Site 2451) Victoria Texas
United States Emerson Clinical Research Institute ( Site 2457) Washington District of Columbia
United States TPMG Clinical Research ( Site 2495) Williamsburg Virginia
United States Clinical Site Partners, LLC d/b/a CSP Miami ( Site 2425) Winter Park Florida

Sponsors (1)

Lead Sponsor Collaborator
Merck Sharp & Dohme LLC

Countries where clinical trial is conducted

United States,  Argentina,  Brazil,  Bulgaria,  Colombia,  Dominican Republic,  Egypt,  France,  Guatemala,  Hungary,  Japan,  Kenya,  Malaysia,  Mexico,  Peru,  Philippines,  Romania,  Russian Federation,  South Africa,  Spain,  Thailand,  Turkey,  Ukraine, 

References & Publications (1)

Alpizar SA, Accini J, Anderson DC, Eysa B, Medina-Pinon I, Ohmagari N, Ostrovskyy MM, Aggrey-Amable A, Beck K, Byrne D, Grayson S, Hwang PMT, Lonchar JD, Strizki J, Xu Y, Paschke A, De Anda CS, Sears PS; MOVe-AHEAD study group. Molnupiravir for intra-hous — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Percentage of Participants Who Had Undetectable SARS-CoV-2 in Baseline Nasopharyngeal (NP) Swabs and Developed COVID-19 (Laboratory-Confirmed SARS-CoV-2 Infection With Symptoms) Through Day 14 Percentage of participants who had undetectable SARS-CoV-2 in baseline NP swabs and developed COVID-19 (laboratory-confirmed SARS-CoV-2 infection with symptoms) through Day 14 were reported. Day 14
Primary Percentage of Participants With =1 Adverse Event An AE is any untoward medical occurrence in a clinical study participant, temporally associated with the use of study intervention, whether or not considered related to the study intervention. 29 days
Primary Percentage of Participants Discontinuing From Study Therapy Due to AE An AE is any untoward medical occurrence in a clinical study participant, temporally associated with the use of study intervention, whether or not considered related to the study intervention. Up to 5 days
Secondary Percentage of Participants (Regardless of SARS-CoV-2 in Baseline NP Swabs) Who Developed COVID-19 (Laboratory-Confirmed SARS-CoV-2 Infection With Symptoms) Through Day 14 Participants who experienced targeted symptoms of COVID-19 (e.g., cough, sore throat) and had NP swabs tested for SARS-CoV-2 using reverse-transcription polymerase chain reaction (RT-PCR).Efficacy analysis was conducted on the mITT (modified intent to treat) population consisting of all randomized participants who received at least 1 dose of study intervention. Up to Day 14
Secondary Percentage of Participants Who Had Undetectable SARS-CoV-2 in Baseline NP Swabs and Developed COVID-19 (Laboratory-Confirmed SARS-CoV-2 Infection With Symptoms) Through Day 29 Participants who experienced targeted symptoms of COVID-19 (e.g., cough, sore throat) and had NP swabs tested for SARS-CoV-2 using RT-PCR. The efficacy analysis population was the mITT (modified intent to treat) population consisting of all randomized participants who received at least 1 dose of study intervention. Up to Day 29
Secondary Percentage of Participants Who Had Undetectable SARS-CoV-2 in Baseline NP Swabs and Developed Detectable SARS-CoV-2 in NP Swabs on or Before Day 14 All participants had NP swabs collected at screening and through Day 14 to test for SARS-CoV-2 using RT-PCR. Efficacy analysis was conducted on the mITT (modified intent to treat) population consisting of all randomized participants who received at least 1 dose of study intervention. Up to Day 14
Secondary Percentage of Participants Who Had Detectable SARS-CoV-2 in Baseline NP Swabs and Developed COVID-19 (Laboratory-confirmed SARS-CoV-2 Infection With Symptoms) Through Day 14 Participants who experienced targeted symptoms of COVID-19 (e.g., cough, sore throat) and had NP swabs tested for SARS-CoV-2 using RT-PCR. Efficacy analysis was conducted on the mITT (modified intent to treat) population consisting of all randomized participants who received at least 1 dose of study intervention. Up to Day 14
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