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Characterization of Doxycycline Pharmacokinetics and Adherence

14 de setembro de 2026 atualizado por: HIV Prevention Trials Network

Characterization of Doxycycline Pharmacokinetics and Adherence Post-Single and Repeat Dosing Schemas

The purpose of this study is to evaluate the effect of body changes on doxycycline concentrations for different dosing schedules. This study will involve a single dose phase and a multiple dose phase. Healthy individuals who do not have a sexually transmitted infection (STI), including acute (e.g., gonorrhea or chlamydia) or chronic (e.g., HIV or HSV-2) infections will be enrolled in this study. Study participants will be randomized to a dosing schedule in each phase and come to the research clinic throughout their time on study for sample collection. Study participants that choose to enroll in this study will be enrolled for about 37 days.

Visão geral do estudo

Descrição detalhada

Doxycycline is a Food and Drug Administration (FDA) approved broad-spectrum, second-generation tetracycline antibiotic that is generally well-tolerated and has been widely used as primary prophylaxis for bacterial and parasitic infections. While the pharmacokinetics (PK) of doxycycline in blood are well-described, knowledge gaps exist with intermittent dosing and establishing adherence thresholds for prophylactic use. Further, the multi-compartment distribution of the doxycycline has not been extensively characterized. The purpose of this study will be to characterize pharmacologic parameters for daily and non-daily doxycycline use and establish adherence cutoffs for daily and non-daily use.

Tipo de estudo

Intervencional

Inscrição (Estimado)

16

Estágio

  • Fase 1

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Locais de estudo

    • North Carolina
      • Chapel Hill, North Carolina, Estados Unidos, 27599
        • University of North Carolina at Chapel Hill

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Sim

Descrição

Inclusion Criteria:

  1. Aged 18 to 65 years of age at the time of screening
  2. Able and willing to follow study participation requirements and provide informed consent to take part in the study
  3. Has a non-reactive/negative HIV test results at screening per applicable algorithm
  4. Has and is able to maintain a caput (head) of hair, that has not been chemically treated (defined as hair that has been bleached, permed, relaxed or dyed/colored) and is greater than one centimeter in length for the duration of the study
  5. For females of reproductive potential: Has a negative urine pregnancy test at screening
  6. For females of reproductive potential: Using at least two effective methods of contraception for at least 30 days (inclusive) prior to enrollment and intending to use two effective methods of contraception for the duration of study participation. It is strongly recommended that at least one barrier method (e.g. condoms) in addition to a hormonal contraception method be used. Examples of acceptable and effective methods include:

    1. Hormonal methods (oral pills, vaginal ring, depo, transdermal or implant)
    2. Intrauterine device (IUD) inserted at least 30 days prior to enrollment
    3. Surgical sterilization (of participant or partner(s)) including bilateral tubal ligation or vasectomized male partners
    4. Barrier methods (condom with/without spermicide, sponge, cervical cap, diaphragm)
    5. Self-identifies as having same sex partners
    6. Self-reported sexually abstinent as defined by abstaining from penile-vaginal intercourse for 90 days prior to enrollment and intending to remain sexually abstinent for the duration of study participation
  7. Has access to a smartphone and/or laptop and is able and willing to participate in video-based communications with study staff for directly observed dosing requirements
  8. In good general health, in the opinion of the investigator of record (IoR) or designee and has no medical condition that would adversely impact the conduct of the study (inclusive of self-reported conditions and/or those found upon medical history and examination or in available medical records). This includes, but is not limited to, having an intact, healthy gastrointestinal tract (without damage or functional disruption) and the ability to swallow pills

Exclusion Criteria:

  1. Per participant report, planned or active use of any anticonvulsants at screening and an unwillingness to restrict use of certain medications (iron, antacids, etc.) for the duration of the study
  2. For females of reproductive potential: Pregnant or currently breastfeeding, or intends to become pregnant and/or breastfeed during the study
  3. Has any of the following laboratory abnormalities:

    1. An estimated calculated creatinine clearance (CrCl) less than 60 mL/min by the Cockcroft-Gault formula at screening
    2. Positive for hepatitis B surface antigen (HBsAg) at screening
    3. Has a Grade 2 or higher clinically significant laboratory abnormality as defined by The Division of AIDS Table for Grading the Severity of Adult and Pediatric Adverse Events, Corrected Version 2.1 - July 2017 (exception: a CrCl ≥ 60 mL/min at enrollment is permissible for enrollment)
  4. Per participant reported symptoms or clinical and/or laboratory diagnosis of an active pharyngeal, anorectal, or reproductive tract infection (RTI) requiring treatment at screening and enrollment per current US Centers for Disease Control and Prevention (CDC) guidelines (https://www.cdc.gov/std/treatment-guidelines/default.htm). Infections requiring treatment include Neisseria gonorrhoeae (GC), Chlamydia trachomatis (CT), syphilis, active herpes simplex virus (HSV) lesions, or symptomatic genital warts, chancroid, pelvic inflammatory disease (PID), bacterial vaginosis (BV), symptomatic vaginal candidiasis, and trichomoniasis
  5. Participation in research studies involving drugs, products, or vaccines within 30 days of the enrollment and for the duration of the study
  6. Has donated blood within 8 weeks of enrollment of approximately 1 pint (550 mL)
  7. Has a known allergy (adverse reaction) to any of the components of the study product, including known hypersensitivity to tetracycline-class antibiotics
  8. Prior use of doxycycline or any other tetracycline-class antibiotic within 30 days prior to enrollment
  9. Has an active infection that may be responsive to treatment with doxycycline or another tetracycline antibiotic
  10. Has evidence or history of any other condition (e.g., gastrectomy, seizure disorder), that, in the opinion of the IoR or designee, would make study participation unsafe, complicate interpretation of study outcome data, or otherwise interfere with achieving study objectives

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Ciência básica
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Single-Dose PK Phase- 200mg delayed release (DR) doxycycline tablet
Participants in this arm will take one 200 mg delayed release (DR) doxycycline hyclate tablet
One 200 mg doxycycline hyclate delayed release (DR) tablet
Experimental: Multi-Dose PK Phase- daily dosing (every 24 hours)
Participants randomized to this arm will receive one 200mg doxycycline hyclate delayed release (DR) tablet daily (every 24 hours) for 10 days.
One 200 mg doxycycline hyclate delayed release (DR) tablet every 24 hours
Experimental: Single Dose PK Phase- Two 100mg immediate release (IR) doxycycline tablets
Participants in this arm will take two 100mg immediate release (IR) doxycycline hyclate tablets
Two 100 mg doxycycline hyclate immediate-release (IR) tablets
Experimental: Multi-dose PK Phase- Intermittent (every 72 hours) dosing
Participants randomized to this arm will receive one 200mg doxycycline hyclate delayed release (DR) tablet intermittently (every 72 hours) for 10 days.
One 200 mg doxycycline hyclate delayed release (DR) tablet every 72 hours

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Maximum observed plasma concentration (Cmax) for 200mg doxycycline hyclate after a single dose.
Prazo: 1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Median (IQR) plasma doxycycline hyclate Cmax (ng/mL units)
1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Minimum observed plasma concentration (Cmin) for 200mg doxycycline hyclate after a single dose.
Prazo: 1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Median (IQR) plasma doxycycline hyclate Cmin (ng/mL units)
1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Time to reach maximum plasma concentration (Tmax) of 200mg doxycycline hyclate after a single dose.
Prazo: 1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Median (IQR) plasma doxycycline hyclate Tmax (hours units)
1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Plasma half-life (T1/2) of 200mg doxycycline hyclate after a single dose.
Prazo: 1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Median (IQR) plasma doxycycline hyclate half-life (T1/2, hours units)
1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Area Under the Concentration-Time Curve in plasma From One to 336 Hours After Dosing (AUC0-24) of 200mg doxycycline hyclate.
Prazo: 1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Median (IQR) plasma doxycycline hyclate area under the concentration time curve (AUC)0-inf (ng*hr/mL units)
1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Plasma concentrations at 24 hours (C24) post last dose of doxycycline following 10 days of daily or intermittent dosing.
Prazo: 24 hours post last dose of the multiple dose phase.
Median (IQR) plasma concentration at 24 hours post last dose (ng/mL units)
24 hours post last dose of the multiple dose phase.
Plasma concentrations at 48 hours (C48) post last dose of doxycycline following 10 days of daily or intermittent dosing.
Prazo: 48 hours post last dose of the multiple dose phase.
Median (IQR) plasma concentration at 48 hours post last dose (ng/mL units)
48 hours post last dose of the multiple dose phase.
Plasma concentrations at 72 hours (C72) post last dose of doxycycline following 10 days of daily or intermittent dosing.
Prazo: 72 hours post last doseof the multiple dose phase.
Median (IQR) plasma concentration at 72 hours post last dose (ng/mL units)
72 hours post last doseof the multiple dose phase.

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Number of gastrointestinal (GI)-related adverse events reported after doxycycline hyclate dosing during the multiple dose phase.
Prazo: Study visit days 14-23
Number of GI-related adverse events during 10 days of daily or intermittent doxycycline dosing
Study visit days 14-23
Number of gastrointestinal (GI)-related adverse events reported after doxycycline hyclate dosing after the multiple dose phase.
Prazo: Up to 14 days post last dose.
Number of GI-related adverse events for 14 days following final daily or intermittent dose (through the Final/Day 37 visit)
Up to 14 days post last dose.
Maximum observed dried blood spot (DBS) concentration (Cmax) for 200mg doxycycline hyclate after a single dose.
Prazo: 1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Median (IQR) DBS doxycycline hyclate Cmax (ng/mL units)
1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Minimum observed dried blood spot (DBS) concentration (Cmin) for 200mg doxycycline hyclate after a single dose.
Prazo: 1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Median (IQR) DBS doxycycline hyclate Cmin (ng/mL units)
1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Time to reach maximum dried blood spot (DBS) concentration (Tmax) of 200mg doxycycline hyclate after a single dose.
Prazo: 1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Median (IQR) DBS doxycycline hyclate Tmax (hours units)
1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Dried blood spot (DBS) half-life (T1/2) of 200mg doxycycline hyclate after a single dose.
Prazo: 1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Median (IQR) DBS doxycycline hyclate half-life (T1/2, hours units)
1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Area Under the Concentration-Time Curve in dried blood spots (DBS) From One to 336 Hours After Dosing (AUC0-24) of 200mg doxycycline hyclate.
Prazo: 1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Median (IQR) DBS doxycycline hyclate area under the concentration time curve (AUC)0-inf (ng*hr/mL units)
1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Maximum observed anorectal fluid concentration (Cmax) for 200mg doxycycline hyclate after a single dose.
Prazo: 1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Median (IQR) anorectal doxycycline hyclate Cmax (ng/swab units)
1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Minimum observed anorectal fluid concentration (Cmin) for 200mg doxycycline hyclate after a single dose.
Prazo: 1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Median (IQR) anorectal doxycycline hyclate Cmin (ng/swab units)
1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Time to reach maximum anorectal fluid concentration (Tmax) of 200mg doxycycline hyclate after a single dose.
Prazo: 1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Median (IQR) anorectal doxycycline hyclate Tmax (hours units)
1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Anorectal fluid half-life (T1/2) of 200mg doxycycline hyclate after a single dose.
Prazo: 1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Median (IQR) anorectal doxycycline hyclate half-life (T1/2, hours units)
1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Area Under the Concentration-Time Curve in anorectal fluid From One to 336 Hours After Dosing (AUC0-24) of 200mg doxycycline hyclate.
Prazo: 1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Median (IQR) anorectal doxycycline hyclate area under the concentration time curve (AUC)0-inf (ng*hr/swab units)
1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Maximum observed vaginal fluid concentration (Cmax) for 200mg doxycycline hyclate after a single dose.
Prazo: 1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Median (IQR) vaginal doxycycline hyclate Cmax (ng/swab units)
1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Minimum observed vaginal fluid concentration (Cmin) for 200mg doxycycline hyclate after a single dose.
Prazo: 1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Median (IQR) vaginal doxycycline hyclate Cmin (ng/swab units)
1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Time to reach maximum vaginal fluid concentration (Tmax) of 200mg doxycycline hyclate after a single dose.
Prazo: 1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Median (IQR) vaginal doxycycline hyclate Tmax (hours units)
1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Vaginal fluid half-life (T1/2) of 200mg doxycycline hyclate after a single dose.
Prazo: 1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Median (IQR) vaginal doxycycline hyclate half-life (T1/2, hours units)
1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Area Under the Concentration-Time Curve in vaginal fluid From One to 336 Hours After Dosing (AUC0-24) of 200mg doxycycline hyclate.
Prazo: 1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Median (IQR) vaginal doxycycline hyclate area under the concentration time curve (AUC)0-inf (ng*hr/swab units)
1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Maximum observed pooled urine concentration (Cmax) for 200mg doxycycline hyclate after a single dose.
Prazo: 1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Mean (95% CI) urine doxycycline hyclate Cmax (ng/mL units)
1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Minimum observed pooled urine concentration (Cmin) for 200mg doxycycline hyclate after a single dose.
Prazo: 1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Mean (95% CI) urine doxycycline hyclate Cmin (ng/mL units)
1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Time to reach maximum pooled urine concentration (Tmax) of 200mg doxycycline hyclate after a single dose.
Prazo: 1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Mean (95% CI) urine doxycycline hyclate Tmax (hours units)
1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Pooled urine half-life (T1/2) of 200mg doxycycline hyclate after a single dose.
Prazo: 1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Mean (95% CI) urine doxycycline hyclate half-life (T1/2, hours units)
1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Area Under the Concentration-Time Curve in urine From One to 336 Hours After Dosing (AUC0-24) of 200mg doxycycline hyclate.
Prazo: 1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Mean (95% CI) urine doxycycline hyclate area under the concentration time curve (AUC)0-inf (ng*hr/mL units)
1, 2, 3, 4, 6, 8, 24, 72, 96, 168, 240, and 336 hours post dose.
Dried blood spot (DBS) concentrations at 24 hours (C24) post last dose of doxycycline following 10 days of daily or intermittent dosing.
Prazo: 24 hours post last dose of the multiple dose phase.
Median (IQR) DBS concentration at 24 hours post last dose (ng/mL units)
24 hours post last dose of the multiple dose phase.
Dried blood spot (DBS) concentrations at 48 hours (C48) post last dose of doxycycline following 10 days of daily or intermittent dosing.
Prazo: 48 hours post last dose of the multiple dose phase.
Median (IQR) DBS concentration at 48 hours post last dose (ng/mL units)
48 hours post last dose of the multiple dose phase.
Dried blood spot (DBS) concentrations at 72 hours (C72) post last dose of doxycycline following 10 days of daily or intermittent dosing.
Prazo: 72 hours post last dose of the multiple dose phase.
Median (IQR) DBS concentration at 72 hours post last dose (ng/mL units)
72 hours post last dose of the multiple dose phase.
Urine concentrations at 24 hours (C24) post last dose of doxycycline following 10 days of daily or intermittent dosing.
Prazo: 24 hours post last dose of the multiple dose phase.
Median (IQR) urine concentration at 24 hours post last dose (ng/mL units)
24 hours post last dose of the multiple dose phase.
Urine concentrations at 48 hours (C48) post last dose of doxycycline following 10 days of daily or intermittent dosing.
Prazo: 48 hours post last dose of the multiple dose phase.
Median (IQR) urine concentration at 48 hours post last dose (ng/mL units)
48 hours post last dose of the multiple dose phase.
Urine concentrations at 72 hours (C72) post last dose of doxycycline following 10 days of daily or intermittent dosing.
Prazo: 72 hours post last dose of the multiple dose phase.
Median (IQR) urine concentration at 72 hours post last dose (ng/mL units)
72 hours post last dose of the multiple dose phase.
Anorectal fluid concentrations at 24 hours (C24) post last dose of doxycycline following 10 days of daily or intermittent dosing.
Prazo: 24 hours post last dose of the multiple dose phase.
Median (IQR) anorectal concentration at 24 hours post last dose (ng/swab units)
24 hours post last dose of the multiple dose phase.
Anorectal fluid concentrations at 48 hours (C48) post last dose of doxycycline following 10 days of daily or intermittent dosing.
Prazo: 48 hours post last dose of the multiple dose phase.
Median (IQR) anorectal concentration at 48 hours post last dose (ng/swab units)
48 hours post last dose of the multiple dose phase.
Anorectal fluid concentrations at 72 hours (C72) post last dose of doxycycline following 10 days of daily or intermittent dosing.
Prazo: 72 hours post last dose of the multiple dose phase.
Median (IQR) anorectal concentration at 72 hours post last dose (ng/swab units)
72 hours post last dose of the multiple dose phase.
Vaginal fluid concentrations at 24 hours (C24) post last dose of doxycycline following 10 days of daily or intermittent dosing.
Prazo: 24 hours post last dose of the multiple dose phase.
Median (IQR) vaginal concentration at 24 hours post last dose (ng/swab units)
24 hours post last dose of the multiple dose phase.
Vaginal fluid concentrations at 48 hours (C48) post last dose of doxycycline following 10 days of daily or intermittent dosing.
Prazo: 48 hours post last dose of the multiple dose phase.
Median (IQR) vaginal concentration at 48 hours post last dose (ng/swab units)
48 hours post last dose of the multiple dose phase.
Vaginal fluid concentrations at 72 hours (C72) post last dose of doxycycline following 10 days of daily or intermittent dosing.
Prazo: 72 hours post last dose of the multiple dose phase.
Median (IQR) vaginal concentration at 72 hours post last dose (ng/swab units)
72 hours post last dose of the multiple dose phase.

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Investigadores

  • Cadeira de estudo: Mackenzie Cottrell, PharmD, MS, University of North Carolina, Chapel Hill
  • Cadeira de estudo: Mark Marzinke, PhD, Johns Hopkins University

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

27 de agosto de 2026

Conclusão Primária (Estimado)

1 de julho de 2027

Conclusão do estudo (Estimado)

1 de julho de 2027

Datas de inscrição no estudo

Enviado pela primeira vez

5 de agosto de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

5 de agosto de 2026

Primeira postagem (Real)

10 de agosto de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

17 de setembro de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

14 de setembro de 2026

Última verificação

1 de setembro de 2026

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • HPTN 117
  • UM1AI068619 (Concessão/Contrato do NIH dos EUA)

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

SIM

Descrição do plano IPD

For studies within two years of primary objective(s) publication, de-identified individual participant data that underlie results in a publication, will be provided upon request. For studies more than two years from the primary objective(s) publication, de-identified datasets will be available upon request (Public Use Datasets).

Prazo de Compartilhamento de IPD

Investigators may request de-identified datasets in order to duplicate published results, as required by specific journals. Otherwise, de-identified datasets will be made available upon request, two years following publication of the primary results manuscript.

Critérios de acesso de compartilhamento IPD

Researchers may submit a request for access to data that has informed published results, by sending an email to HPTN-Data-Access@scharp.org. To access available de-identified datasets, investigators must complete the request form on the Atlas website. Researchers of approved requests will need to sign an HPTN Data Use Agreement before receiving the data and agree to use the provided acknowledgement statement.

Tipo de informação de suporte de compartilhamento de IPD

  • PROTOCOLO DE ESTUDO
  • SEIVA

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Sim

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

produto fabricado e exportado dos EUA

Não

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