Pre-Exposure Prophylaxis Study of Lenacapavir in Cisgender Men, Transgender Women, Transgender Men, and Gender Nonbinary People at Risk for HIV Infection (PURPOSE 2)
Uno studio di fase 3, in doppio cieco, multicentrico, randomizzato per valutare l'efficacia e la sicurezza del lenacapavir sottocutaneo due volte all'anno ad azione prolungata per la profilassi pre-esposizione all'HIV negli uomini cisgender, nelle donne transgender, negli uomini transgender e nelle persone non binarie di genere ≥ 16 anni di Età che hanno rapporti sessuali con partner maschili e sono a rischio di infezione da HIV
The goal of this study is to evaluate the efficacy of the study drugs, lenacapavir (LEN) in preventing HIV infection, in participants ≥ 16 years of age who have condomless receptive anal sex with partners assigned male at birth and are at risk for HIV-1 infection.
The primary objective of this study is to evaluate the efficacy of LEN for HIV-1 pre-exposure prophylaxis (PrEP) in participants ≥ 16 years of age who have condomless receptive anal sex with partners assigned male at birth at risk of HIV-1 infection.
Panoramica dello studio
Stato
Tipo di studio
Iscrizione (Effettivo)
Fase
- Fase 3
Contatti e Sedi
Luoghi di studio
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Buenos Aires, Argentina, 1072
- Hospital General de Agudos JM Ramos Mejia
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Buenos Aires, Argentina, B7600
- Instituto de Investigaciones Clinicas Mar del Plata
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Buenos Aires, Argentina, 1202
- Fundacion Huesped
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Belo Horizonte - MG, Brasile, 30130-100
- Unidade de Pesquisa Clinica em Vacinas (UPqVac) da Faculdade de Medicina da Universidade
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Canela-Salvador, Brasile, 40110-060
- Fundação Bahiana de Infectologia
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Manauas, Brasile, 69040-000
- Fundação de Medicina Tropical Doutor Heitor Vieira Dourado / Fundação Medicina Tropical do Amazonas - FMT/IMT/AM
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Nova Iguaçu, Brasile, 26030-380
- Hospital General de Nova Iguaçu - HGNI
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Porto Alegre, Brasile, RS 91350 200
- Grupo Hospitalar Conceição/ Hospital Nossa Senhora da Conceição S.A.
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Rio de Janeiro, Brasile, 21040-360
- Instituto Nacional de Infectologia Evandro Chagas / Fundação Oswaldo Cruz - INI FIOCRUZ
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São Paulo, Brasile, 01246-903
- Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo
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São Paulo, Brasile, 04121-000
- Centro de Referência e Treinamento DST/AIDS
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São Paulo, Brasile, 06519-332
- Center for Management and Research. SPDM-Paulista Association for the Development of Medicine-Hospital São Paulo/Federal
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Guadalajara C.P., Messico, 44160
- Centro de Investigacion Farmaceutica Especializada de Occidente S.C.
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Barranco, Perù, 15063
- Asociacion Civil Impacta Salud y Educacion - Sede Barranco
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Callao, Perù, 7006
- Instituto de Medicina Tropical "Daniel Alcides Carrion", Facultad de Medicina Humana, UNMSM
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Iquitos, Perù
- Asociacion Civil Selva Amazonica
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Lima, Perù, 15001
- Via Libre
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Lima, Perù, 15088
- Asociacion Civil Impacta Salud y Educacion - Sede San Miguel
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PR
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San Juan, PR, Porto Rico, 00717
- Ararat Research Center
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San Juan, PR, Porto Rico, 00909
- Centro Ararat- San Juan
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Alabama
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Birmingham, Alabama, Stati Uniti, 35233
- UAB Sexual Health Research Clinic
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California
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Loma Linda, California, Stati Uniti, 92354
- Loma Linda University Clinical Trial Center Clinic
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Los Angeles, California, Stati Uniti, 90069
- Mills Clinical Research
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Los Angeles, California, Stati Uniti, 90036
- Ruane Clinical Research Group Inc.
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Los Angeles, California, Stati Uniti, 90038
- UCLA CBAM Vine Street Clinic
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Los Angeles, California, Stati Uniti, 90059
- Charles R. Drew University of Medicine and Science (CDU) - Clinical Translational Research Center (CTRC)
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Los Angeles, California, Stati Uniti, 90502
- The Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center
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Palm Springs, California, Stati Uniti, 92262
- BIOS Clinical Research
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San Diego, California, Stati Uniti, 92103
- UCSD Anti Viral Research Center
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San Francisco, California, Stati Uniti, 94102
- Optimus Medical Group
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San Francisco, California, Stati Uniti, 94102
- Bridge HIV at the San Francisco Department of Public Health
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Colorado
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Aurora, Colorado, Stati Uniti, 80045
- University of Colorado Clinical and Translational Research Centers (CTRC)
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Connecticut
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New Haven, Connecticut, Stati Uniti, 06510
- Yale University, School of Medicine
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District of Columbia
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Washington D.C., District of Columbia, Stati Uniti, 20009
- Whitman-Walker Institute Inc.
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Washington D.C., District of Columbia, Stati Uniti, 20017
- Washington Health Institute
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Florida
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Fort Lauderdale, Florida, Stati Uniti, 33308
- Therafirst Medical Center
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Fort Lauderdale, Florida, Stati Uniti, 33316
- Gary Richmond, MD, PA
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Ft. Pierce, Florida, Stati Uniti, 34982
- Midway Immunology & Research Center, LLC
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Jacksonville, Florida, Stati Uniti, 32207
- CAN Community Health Clinic
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Miami, Florida, Stati Uniti, 33136
- University of Miami Miller School of Medicine Division of Infectious Disease Research - Converge Miami
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Miami Gardens, Florida, Stati Uniti, 33055
- CAN Community Health
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Orlando, Florida, Stati Uniti, 32803
- Orlando Immunology Center
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Sarasota, Florida, Stati Uniti, 34237
- CAN Community Health
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Georgia
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Atlanta, Georgia, Stati Uniti, 30303
- Emory University
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Atlanta, Georgia, Stati Uniti, 30308
- Emory University Hospital Midtown Infectious Disease Clinic
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Atlanta, Georgia, Stati Uniti, 30030
- The Hope Clinic at Emory University
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Illinois
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Chicago, Illinois, Stati Uniti, 60613
- Howard Brown Health Center
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Chicago, Illinois, Stati Uniti, 60612
- RMR Core Center
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Chicago, Illinois, Stati Uniti, 60612
- University of Illinois at Chicago, Department of Medicine, Division of Infectious Diseases, Project WISH
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Indiana
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Indianapolis, Indiana, Stati Uniti, 46202
- Indiana University Infectious Diseases Research
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Kentucky
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Lexington, Kentucky, Stati Uniti, 40503
- Baptist Health Lexington
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Louisville, Kentucky, Stati Uniti, 40241
- Norton Infectious Disease Specialists
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Louisiana
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New Orleans, Louisiana, Stati Uniti, 70119
- LSU-CrescentCare Sexual Health Center- New Orleans Community Health Center
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Maryland
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Baltimore, Maryland, Stati Uniti, 21287
- Johns Hopkins University School of Medicine
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Massachusetts
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Boston, Massachusetts, Stati Uniti, 02215
- The Fenway Institute
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Michigan
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Berkley, Michigan, Stati Uniti, 48072
- Be Well Medical Center
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Detroit, Michigan, Stati Uniti, 48202
- Henry Ford Hospital
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Mississippi
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Jackson, Mississippi, Stati Uniti, 39202
- Open Arms Healthcare Center
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Missouri
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Kansas City, Missouri, Stati Uniti, 64111
- KC CARE Health Center
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New Jersey
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Newark, New Jersey, Stati Uniti, 07102
- St. Michael's Medical Center
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Somers Point, New Jersey, Stati Uniti, 08244
- South Jersey Infectious Disease
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New York
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New York, New York, Stati Uniti, 10029
- Icahn School of Medicine at Mount Sinai- Mount Sinai Downtown
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North Carolina
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Chapel Hill, North Carolina, Stati Uniti, 27514
- NC TraCS Institute - CTRC; University of North Carolina at Chapel Hill
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Greensboro, North Carolina, Stati Uniti, 27401
- Cone Health/Regional Center for Infectious Disease Research Center
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Winston-Salem, North Carolina, Stati Uniti, 27103
- Wake Forest University Health Sciences
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Ohio
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Cincinnati, Ohio, Stati Uniti, 45267
- University of Cincinnati
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Columbus, Ohio, Stati Uniti, 43210
- The Ohio State University Wexner Medical Center
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Pennsylvania
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Philadelphia, Pennsylvania, Stati Uniti, 19104
- Penn Prevention Unit
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Philadelphia, Pennsylvania, Stati Uniti, 19107
- Philadelphia FIGHT Community Health Centers, Jonathan Lax Treatment Center
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South Carolina
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Charleston, South Carolina, Stati Uniti, 29425
- Medical University of South Carolina, Infectious Disease Clinic
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Columbia, South Carolina, Stati Uniti, 29203
- Prisma Health-Midlands Clinical Research Unit
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Greenville, South Carolina, Stati Uniti, 29605
- Prisma Health Internal Medicine Clinic
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Tennessee
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Memphis, Tennessee, Stati Uniti, 38105
- St Jude Children's Research Hospital
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Memphis, Tennessee, Stati Uniti, 38103
- Methodist University Hospital/University of Tennessee Health Science Center, Clinical Research Center
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Nashville, Tennessee, Stati Uniti, 37208
- Meharry Medical College Clinical and Transitional Research Center
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Texas
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Austin, Texas, Stati Uniti, 78705
- Central Texas Clinical Research
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El Paso, Texas, Stati Uniti, 79915
- Centro San Vincente
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Houston, Texas, Stati Uniti, 77098
- The Crofoot Research Center, INC
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Houston, Texas, Stati Uniti, 77009
- UT Health Science Center at Houston
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Washington
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Seattle, Washington, Stati Uniti, 98104
- Ofiice of Dr. Peter Shalit, MD
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Cape Town, Sud Africa, 7925
- Desmond Tutu Health Foundation
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Johannesburg, Sud Africa, 2038
- Wits Reproductive Health and HIV Institute (Wits RHI)
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Pretoria, Sud Africa, 87
- The Aurum Institute: Pretoria Clinical Research Centre
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Soshanguvhe, Sud Africa, 0152
- Setshaba Research Centre
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Tembisa, Sud Africa, 1632
- The Aurum Institute Tembisa CRC, Clinic 4
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Vincent, Sud Africa, 5217
- FPD-DTHF Ndevana Commuity Research Site
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Bangkok, Tailandia, 10330
- King Chulalongkorn Memorial Hospital
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Bangkok, Tailandia, 10400
- Ramathibodi Hospital, Mahidol University
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Bangkok, Tailandia, 10330
- Institute of HIV Research and Innovation
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Bangkok, Tailandia, 10330
- The HIV Netherlands Australia Thailand Research Collaboration (HIV-NAT), Thai Red Cross AIDS research Centre
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Chiang Mai, Tailandia, 50200
- Research Institute for Health Sciences, Chiang Mai University
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Khon Kaen, Tailandia, 40002
- Srinagarind Hospital, Khon Kaen University
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Nonthaburi, Tailandia, 11000
- Bamrasnaradura Infectious Disease Institute
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Key Inclusion Criteria:
Incidence Phase
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CGM, TGW, TGM, and GNB who have condomless receptive anal sex with partners assigned male at birth and are at risk for HIV infection.
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HIV-1 status unknown at screening and no prior HIV-1 testing within the last 3 months.
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Sexually active with ≥ 1 partner assigned male at birth (condomless receptive anal sex) in the last 12 months and 1 of the following:
- Condomless receptive anal sex with ≥ 2 partners in the last 12 weeks.
- History of syphilis, rectal gonorrhea, or rectal chlamydia in the last 24 weeks.
- Self-reported use of stimulants with sex in the last 12 weeks.
Randomized Phase
- Negative local rapid fourth generation HIV-1/2 Ab/Ag, central fourth generation HIV-1/2 Ab/Ag, and HIV-1 RNA quantitative nucleic acid amplification testing (NAAT).
- Estimated glomerular filtration rate (eGFR) ≥ 60 mL/min at screening according to the Cockcroft-Gault formula for creatinine clearance (CLcr).
Key Exclusion Criteria:
Incidence Phase
- Prior use of HIV PrEP (including F/TDF or F/TAF) or HIV postexposure prophylaxis (PEP) in the past 12 weeks or any prior use of long-acting systemic PrEP (including cabotegravir or islatravir).
- Prior recipient of an HIV vaccine or HIV broadly neutralizing antibody formulation.
Randomized Phase
- Acute viral hepatitis A, B or C or evidence of chronic hepatitis B or C infection.
- Severe hepatic impairment or a history of or current clinical decompensated liver cirrhosis.
Note: Other protocol defined Inclusion/Exclusion criteria may apply.
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Prevenzione
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Doppio
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
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Sperimentale: Randomized Blinded Phase: LEN + Placebo-to-match (PTM) F/TDF
Participants will receive the following for up to approximately 52 weeks:
Participants will receive oral LEN if SC injections are not available. |
Tablets administered orally without regard to food
Altri nomi:
Administered via SC injections
Altri nomi:
Tablets administered orally |
|
Sperimentale: Randomized Blinded Phase: Placebo LEN + F/TDF
Participants will receive the following for up to approximately 52 weeks:
Participants will receive oral LEN placebo if SC injections are not available. |
Tablets administered orally
Altri nomi:
Administered via SC injections Tablets administered orally |
|
Sperimentale: LEN Open-Label Extension (OLE) Phase
Participants will be offered entry into LEN OLE Phase, following completion of primary analysis, if LEN demonstrates acceptable safety and efficacy in the Randomized Blinded Phase. Participants randomized to LEN will continue to receive SC LEN 927 mg, every 26 weeks (± 7 days), and have study visits every 13 weeks (± 7 days). Participants randomized to F/TDF will switch to SC LEN 927 mg on OLE Day 1, Week 26 and every 26 weeks thereafter. Participants will also receive oral LEN 600 mg on OLE Days 1 and 2. All participants in LEN OLE Phase will complete the phase, once LEN becomes available or the sponsor decides to discontinue the study, whichever happens first. After completing LEN OLE Phase or study discontinuation, participants will transition to local PrEP, including LEN or other options. If a participant exits early, they will complete an early study drug discontinuation (ESDD), be referred to local PrEP services if needed, and have a 30-day follow-up visit. |
Tablets administered orally without regard to food
Altri nomi:
Administered via SC injections
Altri nomi:
|
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Sperimentale: Pharmacokinetic (PK) Tail Phase
Participants who prematurely discontinue study drug during the Randomized Blinded Phase and participants that were randomized to LEN who choose not to continue in the LEN OLE Phase will transition to the PK Tail Phase. Participants will receive oral F/TDF (or Emtricitabine/Tenofovir Alafenamide (F/TAF) for US participants only) once daily for 78 weeks to cover the PK tail and complete visits every 13 weeks (+/- 7 days). Upon unblinding, participants who were randomized to F/TDF in the Randomized Blinded Phase who decline to participate in the LEN OLE Phase will complete the ESDD visit, transition to local HIV prevention services, and return for a 30-day follow-up visit. |
Tablets administered orally
Altri nomi:
F/TAF tablets administered orally once daily
Altri nomi:
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Incidence Phase: Recent Infection Testing Algorithm (RITA) Estimate of the Background Human Immunodeficiency-1 Virus Infection Incidence Rate (bHIV) Per 100 Person Years (PY)
Lasso di tempo: Incidence Phase Screening Visit (Day 1)
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bHIV per 100 PY in the Incidence Phase was calculated using RITA. The RITA incorporated HIV-1 testing results and recency assay testing results to estimate the bHIV. Recency assay testing was performed for participants in the All Screened Set found to have HIV-1 infection at the Incidence Phase Screening Visit as defined below. Participants were considered to have recent HIV-1 infection if the normalized optical density (ODn) was below 1.5 threshold using the Sedia limiting antigen avidity enzyme immunoassay (LAg-EIA) and the HIV-1 RNA (viral load) was > 75 copies/mL of blood. HIV-1 infection was defined as participants having at least one of the following central lab results at the Incidence Phase screening visit:
|
Incidence Phase Screening Visit (Day 1)
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Randomized Blinded Phase: HIV-1 Incidence Reported Per 100 PY for LEN Compared to Background HIV (bHIV, Participants in All Screened Set)
Lasso di tempo: Up to 149 weeks
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HIV-1 incidence per 100 PY for LEN was calculated as the number of participants who acquired HIV-1 divided by the total of a) for participants not diagnosed with HIV-1, sum of all duration of follow-up time in years, while at risk of HIV-1 infection (where a year is 365.25 days) and b) for participants diagnosed with HIV-1, sum of all duration of follow-up time up to confirmed HIV-1 diagnoses. HIV-1 diagnosis was determined by an HIV adjudication committee who reviewed potential HIV-1 infection events in the randomized participants. The committee, in a blinded, consistent, and unbiased manner, determined whether HIV test results confirmed HIV-1 infection and determined the date of diagnosis for each case, defined as the date of the earliest study visit with evidence of HIV infection considering both prospective HIV testing and back-testing of archived samples. bHIV incidence per 100 PY in All Screened Set was estimated as described in outcome measure#1. |
Up to 149 weeks
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Randomized Blinded Phase: HIV-1 Incidence Reported Per 100 PY for LEN Compared to F/TDF
Lasso di tempo: Up to 149 weeks
|
HIV-1 incidence per 100 PY was calculated as the number of participants who acquired HIV-1 divided by the total of a) for participants not diagnosed with HIV-1, sum of all duration of follow-up time in years, while at risk of HIV-1 infection (where a year is 365.25 days) and b) for participants diagnosed with HIV-1, sum of all duration of follow-up time up to confirmed HIV-1 diagnoses. HIV-1 diagnosis was determined by an HIV adjudication committee who reviewed potential HIV-1 infection events in the randomized participants. The committee, in a blinded, consistent, and unbiased manner, determined whether HIV test results confirmed HIV-1 infection and determined the date of diagnosis for each case, defined as the date of the earliest study visit with evidence of HIV infection considering both prospective HIV testing and back-testing of archived samples. |
Up to 149 weeks
|
|
Randomized Blinded Phase: HIV-1 Incidence Among Participants Adherent to LEN
Lasso di tempo: Up to 149 weeks
|
A participant was defined as adherent to LEN if they have received all per-protocol administrations of LEN within 28 weeks since the previous administration. The incidence of HIV-1 infection per 100 PY calculation is defined in outcome measure #2. |
Up to 149 weeks
|
|
Randomized Blinded Phase: Percentage of Participants Experiencing Treatment-Emergent Adverse Events (TEAEs)
Lasso di tempo: First dose date up to 184 weeks
|
An adverse event (AE) was any untoward medical occurrence in a clinical study participant administered a study drug that did not necessarily have a causal relationship with the treatment. TEAEs were defined as 1 or both of the following: Any AEs leading to premature discontinuation of study drug, or any AEs with an onset date on or after the study drug start date and no later than the last exposure date after permanent discontinuation of the study drug. |
First dose date up to 184 weeks
|
|
Randomized Blinded Phase: Percentage of Participants Experiencing Grade 3 or Higher Laboratory Abnormalities
Lasso di tempo: First dose date up to 184 weeks
|
Treatment-emergent laboratory abnormalities were defined as values that increased at least 1 toxicity grade from baseline at any post-baseline visit, up to and including the last exposure date for participants who permanently discontinued study drug, or the last available date in the database snapshot for participants who were still on treatment at the time of an analysis. The division of acquired immunodeficiency syndrome toxicity grading scale, Version 2.1 was used to assign toxicity grades (0 to 4) to laboratory results for analysis. Grade 0 included all values that do not meet the criteria for an abnormality of at least Grade 1. Grade 1 mild, Grade 2 moderate, Grade 3 severe, and Grade 4 potentially life-threatening. Percentages were rounded off. |
First dose date up to 184 weeks
|
Collaboratori e investigatori
Sponsor
Investigatori
- Direttore dello studio: Gilead Study Director, Gilead Sciences
Pubblicazioni e link utili
Pubblicazioni generali
- Kelley CF, Acevedo-Quiñones M, Agwu AL, et al. Twice-yearly lenacapavir PrEP in cisgender gay men, transgender women and men, and gender-diverse people (PURPOSE 2). Presented at: HIV Drug Therapy Glasgow; November 10-13, 2024; Glasgow, United Kingdom.
- Kelley CF, Acevedo-Quinones M, Agwu AL, Avihingsanon A, Benson P, Blumenthal J, Brinson C, Brites C, Cahn P, Cantos VD, Clark J, Clement M, Creticos C, Crofoot G, Diaz RS, Doblecki-Lewis S, Gallardo-Cartagena JA, Gaur A, Grinsztejn B, Hassler S, Hinojosa JC, Hodge T, Kaplan R, Lacerda M, LaMarca A, Losso MH, Valdez Madruga J, Mayer KH, Mills A, Mounzer K, Ndlovu N, Novak RM, Perez Rios A, Phanuphak N, Ramgopal M, Ruane PJ, Sanchez J, Santos B, Schine P, Schreibman T, Spencer LY, Van Gerwen OT, Vasconcelos R, Vasquez JG, Zwane Z, Cox S, Deaton C, Ebrahimi R, Wong P, Singh R, Brown LB, Carter CC, Das M, Baeten JM, Ogbuagu O; PURPOSE 2 Study Team. Twice-Yearly Lenacapavir for HIV Prevention in Men and Gender-Diverse Persons. N Engl J Med. 2025 Apr 3;392(13):1261-1276. doi: 10.1056/NEJMoa2411858. Epub 2024 Nov 27.
- Cespedes M, Das M, Hojilla JC, Blumenthal J, Mounzer K, Ramgopal M, Hodge T, Torres TS, Peterson C, Shibase S, Elliott A, Demidont AC, Callaghan L, Watson CC, Carter C, Kintu A, Baeten JM, Ogbuagu O. Proactive strategies to optimize engagement of Black, Hispanic/Latinx, transgender, and nonbinary individuals in a trial of a novel agent for HIV pre-exposure prophylaxis (PrEP). PLoS One. 2022 Jun 3;17(6):e0267780. doi: 10.1371/journal.pone.0267780. eCollection 2022.
- Cantos Lucio VD, Mngadi K, Supparatpinyo K, et al. From Breakthroughs to Backbones: The Evolving Landscape of HIV PrEP. Presented at: Conference on Retroviruses and Opportunistic Infections (CROI 2026); February 22-25, 2026; Denver, CO. Abstract 129.
- Kwan TH, Chan DPC, Lee SS. Utilisation of HIV pre-exposure prophylaxis and preferences of alternative long-acting modalities among men who have sex with men in Hong kong: a cross-sectional study. BMC Public Health. 2025 Dec 26;26(1):361. doi: 10.1186/s12889-025-26025-5.
Collegamenti utili
Studiare le date dei record
Studia le date principali
Inizio studio (Effettivo)
Completamento primario (Effettivo)
Completamento dello studio (Stimato)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
- Prodotti chimici organici
- Composti eterociclici, 1-anello
- Composti eterociclici
- Composti eterociclici, 2 anelli
- Composti eterociclici, anello fuso
- Preparati farmaceutici
- Acidi nucleici, nucleotidi e nucleosidi
- Purine
- Deossictidina
- Citidina
- Nucleosidi di pirimidina
- Pirimidine
- Composti organofosfori
- Nucleosidi
- Deossiribonucleosidi
- Organofosfonati
- Adenina
- Combinazioni di droga
- Tenofovir
- Emtricitabina
- Combinazione di farmaci Emtricitabina, Tenofovir disoproxil fumarato
- Lenacapavir
- emtricitabine tenofovir alafenamide
Altri numeri di identificazione dello studio
- GS-US-528-9023
- DOH-27-102021-6681 (Altro identificatore: South African National Clinical Trial Registry)
- 2023 (Sovvenzione/contratto NIH degli Stati Uniti)
- 2023-001025-23 (Numero EudraCT)
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Informazioni su farmaci e dispositivi, documenti di studio
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Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .