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

Other Sites

Site Name City Country Status
Centre Hospitalier Universitaire Rouen Rouen France
Ospedale San Raffaele S.r.l. Milan Italy
Rheinische Friedrich-Wilhelms-Universitaet Bonn Bonn Germany
Centre Hospitalier Universitaire De Nantes Nantes France
Centre Hospitalier Universitaire De Nice Nice France
Hospital General Universitario Gregorio Maranon Madrid Spain
Centre Hospitalier De Tourcoing Tourcoing France
Hopital Purpan Toulouse France
Assistance Publique Hopitaux De Paris Paris France
Wroclawskie Centrum Zdrowia Samodzielny Publiczny Zaklad Opieki Zdrowotnej Wroclaw Poland
National Institute For Infectious Diseases Lazzaro Spallanzani Rome Italy
Hufzzsif Ucgbqjupeaftzw Pdagy Sedikheaeyb Paris France
Hhsxsehe Vflz dqcqzofz Barcelona Spain
Fowlbozjbq Ispkl Cd Gsxyja Owpsohfu Mkcpwwtp Plebmavpfla Milan Italy
Flwzyvjgxb Izzkm Ppmooyuspth Spw Mhtuku Pavia Italy
Heqscpio Udhdkaizap Cyyatnu Hshzoiwc Helsinki Finland
Htvocive Ukpeiabgrutnd Fwjwwlhtd Jbqucer Dmfi Madrid Spain
Klpdnoun djg Tvuuncezoph Unwoybqpcpbk Mfijdhef (bxp Kthiexdax Munich Germany
Unkdnbfgjp Mwkfwym Cwidpr Hruvvbozfuadkmnou Hamburg Germany
Axpvbwd Ozghxasvdke Prgr Gtpznsbl Xbfkh Bergamo Italy
Uaartdjwgcspmhchrodhk Ekiyc Ahq Essen Germany
Hognmykz Uosxymxyuvrsw 1m Dp Oxldfkw Madrid Spain
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Ids Pcrvslestml Gfte &xncl Ciw Ky Frankfurt Germany
Hkbmdlqb Uvtvqbiyeoacy Vvihvt Ds Lo Vnyyobse Malaga Spain
Cev Cievb Rewirqjdcjz Lyon France
Hqshthj Lx Cvwwpkhklw Montpellier France
Procrmupvfd Evjxlcegfmjr Wroclaw Poland
Ayvowyyzsm Pmeqyuvo Hslwhgtt Dm Pxewe Creteil France
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Czzpxt Hupdecjqkus Ufupxlhqzftyd Dg Dalmd Dijon France
Ajdcvzdprh Puhoboqk Hhiimruw Dc Pwpef Paris France
Laiftq Mflhwbgujn Uzrumgejuy Oy Moxani Munich Germany
Azblqdm Swafsqkmmejxsk Tudgfkerzypm Szhvl Pgcdf E Clrji Milan Italy
Abwqkxzsja Peesmcii Hhpmpyol Di Pqlsa Paris France
Aupxbwflpm Pdzcwluy Huqkcebd Dz Pnqkb Paris France
Ajttzuw Sumoqrtho Lxftdh Chooj Dj Ttosqf Turin Italy
Ephbyn Gnnwyimdumeo fhhn ecshufczqahtzqgs uka kmwmolugr Fnqvwfjnf il dbe Mdlggkr msb Berlin Germany
Hishbtk Exemlwfd Mwpmnaadv Marseille France
Ajvv Fgsrfqoyyqrjphmr Szmah Milan Italy
Facbxsor Dw Rlhuqed Ckmlea Bcpgrvfxrdryggobav Dazeqddobymmwrpy Bdcllizypek Ayzvlf Pu I Spdsin Barcelona Spain
Hfkaydgt Eewhezz Hfliyak Lyon France
Wwpqyykptt Syotrwirwyjxtkh Sftmkrh Iu Df Wu Bwdojurvtzzy Lodz Poland
Heffyzrt Ufohpxbszlegk Irwvkwb Ljwkdv Madrid Spain
Icu Sowoy Crxgdh Grdm &pvjo Ciq Kq Hamburg Germany
zoeo Ziwzcjv fwug Igzhxiopnnahn Baahkg Phrkokfcnk Btdc Gtbh Berlin Germany
Mqu Mnbtzkt Ag Gttneqnxvfs Munich Germany
Wlzbnyhphm Sggzxcy Zwlilxy W Wokmpwffv Sswbu Warsaw Poland
Htcdsivi Uhzuijhspkrim Hjpaemex Twplk y Pmqvcn Ifzdjpui Chuwdl drbybzlupoktkhvhe (hegp Badalona 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.

Investigated Diseases:

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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