Characterization of Doxycycline Pharmacokinetics and Adherence
2026年9月14日 更新者: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.
調査の概要
状態
招待による登録
条件
詳細な説明
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.
研究の種類
介入
入学 (推定)
16
段階
- フェーズ 1
連絡先と場所
このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。
研究場所
-
-
North Carolina
-
Chapel Hill、North Carolina、アメリカ、27599
- University of North Carolina at Chapel Hill
-
-
参加基準
研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
はい
説明
Inclusion Criteria:
- Aged 18 to 65 years of age at the time of screening
- Able and willing to follow study participation requirements and provide informed consent to take part in the study
- Has a non-reactive/negative HIV test results at screening per applicable algorithm
- 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
- For females of reproductive potential: Has a negative urine pregnancy test at screening
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:
- Hormonal methods (oral pills, vaginal ring, depo, transdermal or implant)
- Intrauterine device (IUD) inserted at least 30 days prior to enrollment
- Surgical sterilization (of participant or partner(s)) including bilateral tubal ligation or vasectomized male partners
- Barrier methods (condom with/without spermicide, sponge, cervical cap, diaphragm)
- Self-identifies as having same sex partners
- 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
- 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
- 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:
- 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
- For females of reproductive potential: Pregnant or currently breastfeeding, or intends to become pregnant and/or breastfeed during the study
Has any of the following laboratory abnormalities:
- An estimated calculated creatinine clearance (CrCl) less than 60 mL/min by the Cockcroft-Gault formula at screening
- Positive for hepatitis B surface antigen (HBsAg) at screening
- 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)
- 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
- Participation in research studies involving drugs, products, or vaccines within 30 days of the enrollment and for the duration of the study
- Has donated blood within 8 weeks of enrollment of approximately 1 pint (550 mL)
- Has a known allergy (adverse reaction) to any of the components of the study product, including known hypersensitivity to tetracycline-class antibiotics
- Prior use of doxycycline or any other tetracycline-class antibiotic within 30 days prior to enrollment
- Has an active infection that may be responsive to treatment with doxycycline or another tetracycline antibiotic
- 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
研究計画
このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:基礎科学
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的: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
|
|
実験的: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
|
|
実験的: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
|
|
実験的: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
|
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Maximum observed plasma concentration (Cmax) for 200mg doxycycline hyclate after a single dose.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Number of gastrointestinal (GI)-related adverse events reported after doxycycline hyclate dosing during the multiple dose phase.
時間枠:Study visit days 14-23
|
Number of GI-related adverse events during 10 days of daily or intermittent doxycycline dosing
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Study visit days 14-23
|
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Number of gastrointestinal (GI)-related adverse events reported after doxycycline hyclate dosing after the multiple dose phase.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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.
|
協力者と研究者
ここでは、この調査に関係する人々や組織を見つけることができます。
捜査官
- スタディチェア:Mackenzie Cottrell, PharmD, MS、University of North Carolina, Chapel Hill
- スタディチェア:Mark Marzinke, PhD、Johns Hopkins University
研究記録日
これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。
主要日程の研究
研究開始 (実際)
2026年8月27日
一次修了 (推定)
2027年7月1日
研究の完了 (推定)
2027年7月1日
試験登録日
最初に提出
2026年8月5日
QC基準を満たした最初の提出物
2026年8月5日
最初の投稿 (実際)
2026年8月10日
学習記録の更新
投稿された最後の更新 (実際)
2026年9月17日
QC基準を満たした最後の更新が送信されました
2026年9月14日
最終確認日
2026年9月1日
詳しくは
本研究に関する用語
キーワード
その他の研究ID番号
- HPTN 117
- UM1AI068619 (米国 NIH グラント/契約)
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
はい
IPD プランの説明
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).
IPD 共有時間枠
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.
IPD 共有アクセス基準
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.
IPD 共有サポート情報タイプ
- STUDY_PROTOCOL
- SAP
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
はい
米国FDA規制機器製品の研究
いいえ
米国で製造され、米国から輸出された製品。
いいえ
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。