Study on Doravirine and Islatravir for People with HIV-1 Previously Treated with the Same Drug Combination

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What is this study about?

This clinical trial is focused on studying the treatment of HIV-1 infection, a virus that attacks the immune system and can lead to acquired immunodeficiency syndrome (AIDS) if not treated. The study involves a medication that combines two active substances: doravirine and islatravir. These substances are provided in a film-coated tablet form, known by the code name MK-8591A, and are taken orally once a day.

The purpose of this study is to evaluate the safety and tolerability of the doravirine/islatravir combination in participants who have previously received this treatment in earlier studies. Participants will continue to take the medication for a period of time, and researchers will monitor them to gather information about any side effects or adverse events that may occur. The study aims to collect data over a period of up to 96 weeks.

Throughout the study, researchers will also assess the effectiveness of the treatment by measuring the levels of HIV-1 in the blood. This will help determine how well the medication is working to control the virus. The study will provide valuable information on the long-term use of this treatment combination for managing HIV-1 infection.

1 beginning of the trial

Upon joining the study, participants will start taking a medication called doravirine/islatravir.

This medication is provided in the form of a film-coated tablet and is taken orally.

2 medication regimen

Participants will take the doravirine/islatravir tablet once daily.

The dosage for this study is 100 mg of doravirine and 0.25 mg of islatravir.

3 duration of treatment

The treatment will continue for a period of up to 96 weeks.

Participants are expected to adhere to the daily medication schedule throughout this period.

4 monitoring and assessments

Participants will be monitored for any adverse events or side effects during the study.

Regular assessments will be conducted to evaluate the HIV-1 RNA levels in the blood, aiming for levels below 50 copies/mL at Week 96.

5 completion of the trial

At the end of the study period, participants will undergo a final evaluation.

The study aims to assess the overall safety and tolerability of the medication regimen.

Who Can Join the Study?

  • The patient must have HIV-1 infection.
  • The patient is currently taking a specific combination tablet called doravirine/islatravir (DOR/ISL) in certain clinical studies sponsored by Merck Sharp & Dohme (MSD).
  • The patient can be of any gender, both male and female are eligible.
  • The patient must be within the age range of 18 to 65 years old.
  • The study includes individuals who may be considered part of a vulnerable population, which means they might need extra protection or care.

Who Cannot Join the Study?

  • Patients who do not have an HIV-1 infection cannot participate.
  • Patients who are not within the specified age range cannot participate. The age range includes both adults and adolescents.
  • Patients who are not part of the specified clinical trial groups cannot participate.
  • Patients who are not willing to follow the study procedures cannot participate.
  • Patients who are pregnant or breastfeeding cannot participate.
  • Patients who have any other medical condition that the study doctors think might make it unsafe for them to participate cannot participate.

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Site Name City Country Status
Centre Hospitalier Universitaire De Bordeaux Bordeaux France
Fondazione Policlinico Universitario Agostino Gemelli IRCCS Rome Italy
Medizinische Hochschule Hannover Hanover Germany
Bellvitge University Hospital L'hospitalet De Llobregat Spain

Other Sites

Site Name City Country Status
Fondazione IRCCS Policlinico San Matteo Pavia Italy
Hospital Universitario Fundacion Jimenez Diaz Madrid Spain
Azienda Sociosanitaria Territoriale Santi Paolo E Carlo Milan Italy
Assistance Publique Hopitaux De Paris Paris France
Centre Hospitalier Universitaire De Nice Nice France
Epimed Gesellschaft fuer epidemiologische und klinische Forschung in der Medizin mbH Berlin Germany
Assistance Publique Hopitaux De Paris Paris France
Wroclawskie Centrum Zdrowia Samodzielny Publiczny Zaklad Opieki Zdrowotnej Wroclaw Poland
Centre Hospitalier Universitaire Rouen Rouen France
Hopitaux Universitaires Pitie Salpetriere Paris France
Centre Hospitalier De Tourcoing Tourcoing France
Centre Hospitalier Universitaire d’Orléans Orléans France
Assistance Publique Hopitaux De Paris Paris France
Fondazione IRCCS Ca Granda Ospedale Maggiore Policlinico Milan Italy
Ospedale San Raffaele S.r.l. Milan Italy
Ludwig Maximilian University Of Munich Munich Germany
Rheinische Friedrich-Wilhelms-Universitaet Bonn Bonn Germany
Centre Hospitalier Universitaire De Nantes Nantes France
Azienda Sanitaria Locale Citta Di Torino Turin Italy
Klinikum der Technischen Universitaet Muenchen (TUM Klinikum) Munich Germany
National Institute For Infectious Diseases Lazzaro Spallanzani Rome Italy
Hopital Europeen Marseille Marseille France
ASST Fatebenefratelli Sacco Milan Italy
Fundacio De Recerca Clinic Barcelona-Institut D’Investigacions Biomediques August Pi I Sunyer Barcelona Spain
Hospital General Universitario Gregorio Maranon Madrid Spain
Hospital Edouard Herriot Lyon France
Hospital Universitario 12 De Octubre Madrid Spain
Wojewodzki Specjalistyczny Szpital Im Dr Wl Bieganskiego Lodz Poland
Hospital Universitario Infanta Leonor Madrid Spain
Fondazione IRCCS San Gerardo Dei Tintori Monza Italy
ICH Study Center GmbH & Co. KG Hamburg Germany
zibp Zentrum fuer Infektiologie Berlin Prenzlauer Berg GmbH Berlin Germany
MVZ Munchen Am Goetheplatz Munich Germany
Wojewodzki Szpital Zakazny W Warszawie SPZOZ Warsaw Poland
IKF Pneumologie GmbH & Co. KG Frankfurt Germany
Hopital Purpan Toulouse France
Assistance Publique Hopitaux De Paris Creteil France
Hospital Universitario Virgen De La Victoria Malaga Spain
Cfczgv Hgkvkrxornq Utpigzktsvxfs Di Dubhs Dijon France
Amrumgyofh Pfgqkjeg Hnmlirvh Df Pyamh Paris France
Hejpucw Ln Coxjltphfb Montpellier France
Pziuqiboaru Eflmrqzokvei Wroclaw Poland
Hceidjxw Ugbasbbaid Csupgnp Huftmeon Helsinki Finland
Urtemipani Mgexmwg Cinuuq Hspdtqzpiksslnqfl Hamburg Germany
Awckzvk Olduddnorde Pcgo Gydviork Xftqt Bergamo Italy
Uglkwvcpurewekeohdjnn Eshrk Asg Essen Germany
Fwitqupwp Pfnq Lk Ioywlrewfgflz Brrdeuuzb Dqf Hgphhegl Uftsqycpexhlr Lx Pft Madrid Spain
Hdoyrqvj Udgcpsvzubtbq Hbdrzvyt Trzhm y Pvmiwo Ixpsaoig Cmktbd diwcjftknkpwurrsu (xqgr Badalona Spain
Cdm Cdowh Rnstinjgzry Lyon France
Hyikvgmr Vxus dygwgixh Barcelona Spain

Want to learn more about this study or check if you can participate? Contact us.

Trial status

Country Status Recruitment Start
Finland Finland
Not yet recruiting
30.03.2023
France France
Not yet recruiting
30.03.2023
Germany Germany
Not yet recruiting
30.03.2023
Italy Italy
Not yet recruiting
30.03.2023
Poland Poland
Not yet recruiting
30.03.2023
Spain Spain
Not yet recruiting
30.03.2023

Trial locations

Investigated drugs:

Doravirine is a medication used to treat HIV-1 infection. It works by blocking a specific enzyme that the virus needs to multiply, helping to lower the amount of virus in the body. This can improve the immune system and reduce the risk of developing HIV-related illnesses.

Islatravir is another medication used in the treatment of HIV-1 infection. It helps to prevent the virus from multiplying by interfering with its ability to replicate. This can help to control the infection and improve the patient’s overall health by maintaining a stronger immune system.

HIV-1 infection – Human Immunodeficiency Virus Type 1 (HIV-1) infection is a viral condition that targets the immune system, specifically the CD4 cells, which are crucial for immune response. As the virus replicates, it gradually depletes these cells, weakening the body’s ability to fight off infections and diseases. The progression of the infection can lead to a significant reduction in immune function, making the individual more susceptible to opportunistic infections and certain cancers. Over time, if untreated, the infection can advance to Acquired Immunodeficiency Syndrome (AIDS), characterized by a severely compromised immune system. The virus is primarily transmitted through contact with infected bodily fluids, such as blood, semen, vaginal fluids, and breast milk. The progression of the disease can vary greatly among individuals, influenced by factors such as viral load, genetic factors, and overall health.

Trial ID:
2022-502126-40-00
Protocol code:
MK-8591A-054
Trial Phase:
Therapeutic confirmatory (Phase III)

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