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4か月の投与間隔(Q4M)で筋肉内投与される長時間作用型カボテグラビルの新規製剤の薬物動態、安全性、忍容性を評価する研究

2026年9月29日 更新者:ViiV Healthcare

HIV感染のリスクがある青年および成人の参加者を対象に、Q4Mに筋肉内注射されたカボテグラビルLAの新製剤の薬物動態プロファイル、安全性、および忍容性を評価する第2b相単群反復投与試験

This study will evaluate the pharmacokinetics (PK), safety, and tolerability of a new formulation of Cabotegravir (CAB) dosed every 4-months (Q4M) for pre-exposure prophylaxis (PrEP) in participants at risk of HIV-1 acquisition.

調査の概要

状態

積極的、募集していない

条件

介入・治療

研究の種類

介入

入学 (実際)

229

段階

  • フェーズ2

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

    • Alabama
      • Birmingham、Alabama、アメリカ、35222
        • GSK Investigational Site
    • California
      • Los Angeles、California、アメリカ、90069
        • GSK Investigational Site
      • Los Angeles、California、アメリカ、90027
        • GSK Investigational Site
      • Los Angeles、California、アメリカ、90036
        • GSK Investigational Site
      • Los Angeles、California、アメリカ、90035
        • GSK Investigational Site
      • Palm Springs、California、アメリカ、92262
        • GSK Investigational Site
    • Florida
      • Doral、Florida、アメリカ、33172-2513
        • GSK Investigational Site
      • Ft. Pierce、Florida、アメリカ、34982-7148
        • GSK Investigational Site
      • Orlando、Florida、アメリカ、32803-1851
        • GSK Investigational Site
      • West Palm Beach、Florida、アメリカ、33407
        • GSK Investigational Site
    • Illinois
      • Chicago、Illinois、アメリカ、60612-7230
        • GSK Investigational Site
    • Louisiana
      • New Orleans、Louisiana、アメリカ、70112
        • GSK Investigational Site
    • Massachusetts
      • Springfield、Massachusetts、アメリカ、01105
        • GSK Investigational Site
    • Michigan
      • Berkley、Michigan、アメリカ、48072
        • GSK Investigational Site
    • Missouri
      • Kansas City、Missouri、アメリカ、64111
        • GSK Investigational Site
    • Nevada
      • Las Vegas、Nevada、アメリカ、89119
        • GSK Investigational Site
    • New York
      • Hawthorne、New York、アメリカ、10532-2140
        • GSK Investigational Site
      • New York、New York、アメリカ、10029
        • GSK Investigational Site
    • North Carolina
      • Greensboro、North Carolina、アメリカ、27401-1209
        • GSK Investigational Site
    • Ohio
      • Cincinnati、Ohio、アメリカ、45267
        • GSK Investigational Site
      • Columbus、Ohio、アメリカ、43210
        • GSK Investigational Site
    • Pennsylvania
      • Pittsburgh、Pennsylvania、アメリカ、15212
        • GSK Investigational Site
    • Texas
      • Dallas、Texas、アメリカ、75246-2004
        • GSK Investigational Site
      • Fort Worth、Texas、アメリカ、76104
        • GSK Investigational Site
    • Washington
      • Seattle、Washington、アメリカ、98104
        • GSK Investigational Site
      • San Juan、プエルトリコ、909
        • GSK Investigational Site
      • San Juan、プエルトリコ、00909
        • GSK Investigational Site

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

16年歳以上 (子、大人、高齢者)

健康ボランティアの受け入れ

はい

受講資格のある性別

全て

説明

Inclusion Criteria:

  1. At the time of obtaining informed consent, adolescent and adult participants weighing at least 35 kg.
  2. Participants must have a nonreactive HIV test at Screening (rapid test, nonrapid HIV immunoassay, and HIV RNA) and enrollment (a rapid test, nonrapid HIV immunoassay, and HIV RNA).
  3. Participants who are at risk of acquiring HIV, defined as having had anal or vaginal sex in the past 6 months.
  4. Participants who are overtly healthy as determined by medical evaluation by a responsible and experienced physician, including medical history, physical examination, laboratory tests and cardiac monitoring at the time of screening.
  5. No alcohol or substance use that, in the opinion of the study investigator and medical monitor, would interfere with the conduct of the study (e.g., provided by self-report, or found upon medical history and examination or in available medical records).
  6. Participants who have received oral PrEP are eligible, but they must discontinue oral PrEP within 10 days of Day 1 visit.
  7. Male or female at birth, (transgender individuals are not excluded). Contraceptive use should align with local regulations. Participants assigned female at birth must not be pregnant or breastfeeding and must either not be of childbearing potential (POCBP) or use highly effective contraception. A POCBP must have a negative pregnancy test within 30 days before dosing.
  8. Participants must be >=16 years old, of legal age to consent to sexual intercourse, and capable of giving written informed consent. Adolescents must provide written informed assent/consent and/or obtain parental/guardian consent if not of legal age, as per site SOPs and IRB/EC policies.

Exclusion Criteria:

  1. One or more reactive or positive HIV test results at Screening or Enrollment, even if HIV infection was not confirmed.

  2. Participants who are breastfeeding or plan to become pregnant or breastfeed during the study.

  3. Alanine aminotransferase (ALT) >=3 times the upper limit of normal (ULN).

  4. Evidence of active Hepatitis B virus (HBV) infection.

    • Participants positive for HBsAg or HBV DNA are excluded.
    • Participants negative for anti-HBs but positive for anti-HBc (negative HBsAg status) and positive for HBV DNA are excluded.
  5. Unstable liver disease, known biliary abnormalities (with the exception of Gilbert's syndrome or asymptomatic gallstones).

  6. History of clinically relevant hepatitis within last 6 months.

  7. Known history of liver cirrhosis with or without viral hepatitis co-infection.

  8. Participants with Hepatitis C virus (HCV) co-infection will be allowed entry into this study if:

    • Liver enzymes meet entry criteria.

    • HCV Disease has undergone appropriate work-up, and is not advanced, and will not require treatment prior to the primary endpoint (e.g., Month 13).

    • In the event that recent biopsy or imaging data is not available or inconclusive, the Fibrosis 4 (Fib-4) score will be used to verify eligibility:

      i. Fib-4 score greater than (>) 3.25 is exclusionary. ii. Fib-4 scores 1.45 - 3.25 requires Medical Monitor consultation. Fibrosis 4 score Formula: (Age x AST) / (Platelets x (sqr [ ALT]) It is approved by the Medical Monitor.

  9. Estimated glomerular filtration rate of <30 mL/min/1.73 m^2 via CKD-EPIcr_R (2021) method.

  10. Any acute laboratory abnormality at Screening, which, in the opinion of the investigator, would preclude the participant's participation in the study of an investigational compound.

  11. Any verified Grade 4 laboratory abnormality, with the exception of Grade 4 [triglycerides or lipid abnormalities].

  12. Participants determined by the Investigator to have a high risk of seizures, A participant with a prior history of seizure may be considered for enrolment if the Investigator believes the risk of seizure recurrence is low. All cases of prior seizure history should be discussed with the Medical Monitor prior to enrolment.

  13. Participant is currently participating in or has participated in a study with a compound or device that is not commercially available within 30 days of signing informed consent, unless permission from the Medical Monitor is granted.

  14. Presence of any history of allergy/sensitivity to any of the study drug.

  15. Inflammatory skin conditions that compromise the safety of IM injections, per the discretion of the investigator.

  16. Participant has an implant/enhancement (including fillers) at the area of proposed injection (e.g., gluteus medius); or tattoo or other dermatological condition overlying the area for IM (e.g., gluteus medius) or any other area which may significantly interfere with interpretation of injection site reactions.

  17. Current or anticipated need for chronic anti-coagulants or active coagulopathy (primary or iatrogenic) which would contraindicate IM injection.

  18. Ongoing or clinically relevant pancreatitis.

  19. Clinically significant cardiovascular disease or history of clinically significant cardiovascular disease.

  20. All participants will be screened for STIs (e.g., chlamydia, gonorrhea, trichomoniasis, syphilis). Participants with untreated infections are excluded. Participants may be rescreened at least 24 hours after completion of STI treatment.

  21. History or presence of sensitivity to any of the study medications or their components or drugs of their class, or a history of drug or other allergy that, in the opinion of the investigator or Medical Monitor, contraindicates their participation. In addition, if heparin is used during PK sampling, subjects with a history of sensitivity to heparin or heparin-induced thrombocytopenia should not be enrolled.

  22. Ongoing uncontrolled malignancy is excluded, whereas participants who have controlled localized malignancies may be included on agreement between the investigator and the Medical Monitor.

  23. Participants who in the investigator's judgment, poses a significant suicidality risk.

  24. Any pre-existing physical or mental condition (including substance abuse disorder) which, in the opinion of the Investigator or the medical monitor, may interfere with the participant's ability to comply with the dosing schedule and/or protocol evaluations or which may compromise the safety of the participant.

  25. Any condition which, in the opinion of the Investigator or the medical monitor, may interfere with the absorption, distribution, metabolism or excretion of the study drugs or render the participant unable to receive IM medication.

  26. Co-enrollment in any other interventional research study or other concurrent studies which may have interfered with this study (as provided by self-report or other available documentation). Exceptions for non-interventional studies may be made if appropriate after consultation with the Medical Monitor.

  27. Participants receiving any protocol-prohibited medication and who are unwilling or unable to switch to an alternate medication.

  28. Use of antiretroviral therapy (ART) for Postexposure Prophylaxis within the 90 days prior to Day 1.

  29. Use of CAB LA for PrEP at any time prior to Screening.

  30. Exposure to an experimental drug or experimental vaccine within either 28 days, 5 half-lives of the test agent, or twice the duration of the biological effect of the test agent, whichever is longer, prior to the first dose of IP.

  31. Anticipated need for HCV therapy with interferon or any drugs that have potential for adverse drug:drug interactions with study treatment throughout the entire study period.

  32. Treatment with an HIV-1 preventive vaccine within 90 days of Screening.

  33. Participant is unlikely to adhere to the study procedures, keep appointments, is planning to relocate during the study, or remain on study through to its conclusion.

  34. Participants who are considered high-risk, meeting at least one of the following criteria:

    • Participant who has exchanged condomless sex for goods or money within the past 12 months prior to Screening.
    • Participant who has used recreational intravenous drugs within the past 12 months prior to Screening.
    • Participant who has participated in Chemsex practice (such as the use of cocaine, crack cocaine, methamphetamine, ketamine, 3,4-methlenedioxy-methamphetamine, GHB, mephedrone or prescription drugs apart from those prescribed by a licensed provider) within the past 6 months prior to Screening.
    • Participant with any STI in the last 6 months also reporting any partners for condomless sex.
    • Participant who has condomless sex with a serodiscordant partner who has a detectable viral load or is not on ART.
    • Participant with any other behavior assessed by the investigator as high-risk sexual behavior.
  35. Participant has in the last 14 days prior to Screening presented with signs and symptoms, which, in the opinion of the investigator, are suggestive of acute HIV infection. Participants may only be enrolled if clinical suspicion of HIV is ruled out with non-reactive results.

  36. Participant becomes a ward of state (e.g., child in care).

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:他の
  • 割り当て:ランダム化
  • 介入モデル:単一グループの割り当て
  • 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:CAB Group

Participants receive lead-in injections comprising cabotegravir LA during month one and injections of a new formulation of CAB LA at Month 3, Month 5 and every 4 months thereafter to Month 29.

Injections administered IM gluteal.

Injections administered IM gluteal.

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
CAB trough concentrations for target of 1.05 microgram per milliliter (μg/mL) for men and 1.39 μg/mL for women
時間枠:From Month 13 to Month 25

CAB trough concentrations are evaluated at or above the target of 1.05 μg/mL for men and 1.39 μg/mL for women, once steady state has been achieved, but no earlier than Month 13 of the study.

From Month 13 to Month 25

二次結果の測定

結果測定
メジャーの説明
時間枠
HIV感染が確認された参加者の割合
時間枠:33ヶ月目まで
33ヶ月目まで
臨床検査値に異常がある参加者の割合
時間枠:33ヶ月目まで
33ヶ月目まで
検査パラメータに変化があった参加者の割合
時間枠:33ヶ月目まで
33ヶ月目まで
CAB trough concentrations for target of 0.672 μg/mL for men and 0.683 μg/mL for women
時間枠:At Month 1

CAB trough concentrations are evaluated at or above the target of 0.672 μg/mL for men and 0.683 μg/mL for women.

At Month 1
CAB trough concentrations for target of 1.05 μg/mL for men and 1.39 μg/mL for women following loading dose
時間枠:From Month 3 to Month 33

CAB trough concentrations are evaluated at or above the target of 1.05 μg/mL for men and 1.39 μg/mL for women.

From Month 3 to Month 33
CAB plasma concentrations
時間枠:At Day 1, Day 1+1Week (W), Month (M) 1, M1+1W, M2, M3, M3+1W, M4, M5, M5+1W, M6, M7, M8, M9, M9+1W, M10, M11, M13, M13+1W, M17, M17+1W, M21, M25, M29, and M33

Blood samples are collected by visit.

At Day 1, Day 1+1Week (W), Month (M) 1, M1+1W, M2, M3, M3+1W, M4, M5, M5+1W, M6, M7, M8, M9, M9+1W, M10, M11, M13, M13+1W, M17, M17+1W, M21, M25, M29, and M33
CAB trough concentrations for target of 4x PA-IC90
時間枠:At Months 1, 3, 5, 9, 13, 17, 21, 25, 29, and 33

CAB trough concentrations are evaluated at or above the target of 4 times (4x) PA-IC90. PA-IC90 is defined as protein-adjusted concentration at which 90% inhibition of viral replication is achieved.

At Months 1, 3, 5, 9, 13, 17, 21, 25, 29, and 33
Percentage of participants with Study Medication Satisfaction Questionnaire Status version (SMSQs) results
時間枠:From Month 1 up to Month 33

SMSQs is a self-completion measure which is evaluating 11-items (i.e., satisfaction, side effects, demands, convenience, flexibility, understanding, lifestyle, recommend, continue, easy or difficult, discomfort or pain). SMSQs is self-administered at each planned study visit and prior to the study drug administration.

From Month 1 up to Month 33
Percentage of participants with Adverse events (AEs)
時間枠:Up to Month 33

An AE is any untoward medical occurrence in a clinical study participant, temporally associated with the use of a study treatment, whether or not considered related to the study treatment.

Up to Month 33
Percentage of participants with AEs by severity
時間枠:Up to Month 33

Severity is graded according to the Division of Acquired Immunodeficiency Syndrome (DAIDS) grading criteria, where Grade 1 = mild, Grade 2 = moderate, Grade 3 = severe, Grade 4 = potentially life-threatening.

Up to Month 33
Percentage of participants with laboratory abnormalities by severity
時間枠:Up to Month 33

Severity is graded according to the DAIDS grading criteria, where Grade 1 = mild, Grade 2 = moderate, Grade 3 = severe, Grade 4 = potentially life-threatening.

Up to Month 33

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。

スポンサー

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)

2024年12月20日

一次修了 (実際)

2026年9月9日

研究の完了 (推定)

2029年8月30日

試験登録日

最初に提出

2024年12月17日

QC基準を満たした最初の提出物

2024年12月17日

最初の投稿 (実際)

2024年12月19日

学習記録の更新

投稿された最後の更新 (実際)

2026年10月5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29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

その他の研究ID番号

  • 219230
  • 2024-000061-24 (EudraCT番号)

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

Study sponsor will assess requests from qualified researchers for anonymized individual patient-level data and related study documents. Data sharing is subject to certain criteria, conditions, and exceptions. For further information, refer to https://www.viiv-studyregister.com/documents/About_ViiV_Patient_Level_Data_Sharing_Final_25Sep2023.pdf

IPD 共有時間枠

Anonymized IPD will be made available within 6 months of publication of primary, key secondary and safety results for studies in product with approved indication(s) or terminated asset(s) across all indications.

IPD 共有アクセス基準

Anonymized IPD is shared with researchers whose proposals are approved by an Independent Review Panel and after a Data Sharing Agreement is in place. Access is provided for an initial period of 12 months but an extension may be granted, when justified, for up to 6 months.

IPD 共有サポート情報タイプ

  • STUDY_PROTOCOL
  • SAP
  • ICF
  • CSR

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

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。