- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07711210
Efficacy and Safety of the ACC017-Based Antiretroviral Regimen in Treatment-Experienced Adults With HIV-1 Harboring Non-Nucleoside Reverse Transcriptase Inhibitor Resistance Mutations
Efficacy and Safety of the ACC017-Based Antiretroviral Regimen in Treatment-Experienced Adults With HIV-1 Harboring Non-Nucleoside Reverse Transcriptase Inhibitor Resistance Mutations: A Randomized, Double-Blind, Placebo-Controlled Clinical Trial
This trial is a randomized, double-blind, placebo-controlled clinical study conducted in treatment-experienced adults with NNRTI-resistant HIV-1, designed to preliminarily evaluate the efficacy, safety, and resistance profile of the core drug ACC017 in this population.
The study consists of two treatment phases: a functional monotherapy period (double-blind phase) and an extended optimized treatment period (open-label phase).
The first phase is the functional monotherapy period (W1-W2). After initial screening, eligible participants will return to the hospital on D1 for final eligibility review and baseline examinations. Those who pass the review will be randomized in a 2:1 ratio to either ACC017 tablets (N=8, 40 mg, once daily [QD]) or matching placebo (N=4), replacing the core NNRTI drug in the failing background regimen while maintaining the original backbone NRTIs unchanged. Treatment will continue for 2 weeks.
The second phase is the extended optimized treatment period (W3-W16). All participants who complete the functional monotherapy period will receive ACC017 tablets (40 mg QD) in combination with an optimized backbone regimen (i.e., ACC017 replaces the core NNRTI drug in the failing background regimen, while the investigator adjusts the backbone drugs based on HIV genotypic resistance test results to ensure at least one backbone NRTI remains sensitive, if applicable). Treatment will continue for 14 weeks.
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Type d'étude
Inscription (Réel)
Phase
- Phase 2
- La phase 1
Contacts et emplacements
Lieux d'étude
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Shanghai, Chine
- Shanghai Clinical Center for Public Health
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-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
La description
Inclusion Criteria:
Participants must meet all of the following criteria to be eligible for this trial:
- Voluntarily sign the informed consent form before screening and be able to comply with the protocol procedures or agreed requirements;
- Age ≥18 years (inclusive) at the time of signing the informed consent, regardless of gender;
- Diagnosed with HIV-1 infection before screening, having received the current first-line antiretroviral therapy (i.e., one NNRTI combined with two NRTIs) for at least 6 months (changes in treatment regimen due to tolerability issues or other adverse reactions are acceptable), with treatment interruption ≤4 weeks before screening (if applicable);
- Before and at screening, no prior use of INSTI, PI, or other novel antiretroviral drugs (including but not limited to fusion inhibitors [FI] or capsid inhibitors [CAI]), including for pre-exposure prophylaxis (PrEP) and/or post-exposure prophylaxis (PEP);
- At least one HIV-1 RNA test result ≥400 copies/mL within 8 weeks before screening, and confirmed HIV-1 RNA ≥400 copies/mL at screening (with ≥7 days between the two tests); or at least one HIV-1 RNA test result ≥50 copies/mL to <400 copies/mL within 8 weeks before screening, and confirmed HIV-1 RNA ≥1000 copies/mL at screening (with ≥7 days between the two tests);
- Within 8 weeks before or at screening, documented NNRTI resistance mutations in the resistance test results (as interpreted by the Stanford HIVdb database, including "low-level resistance [L]," "intermediate resistance [I]," and "high-level resistance [H]") (if two test results exist, the most recent one shall prevail);
- At screening, based on resistance test results, at least one fully active NRTI backbone drug is available for optimized background therapy in the trial (as interpreted by the Stanford HIVdb database, including "susceptible [S]" and "potential low-level resistance [P]");
- Participants agree not to modify their antiretroviral treatment regimen-including but not limited to the composition, dosage, or frequency of regimen drugs-without the investigator's consent from the time of signing the informed consent until the end of the study.
Exclusion Criteria:
Participants will be excluded from this trial if they meet any of the following criteria:
- The investigator judges that the participant has poor treatment compliance or protocol adherence, or any other condition that makes them unsuitable for participation, or that participation may not maximize the participant's health interests;
- At screening, female participants are pregnant or breastfeeding, or male/female participants engaging in heterosexual activity plan to conceive (including sperm/egg donation) from 1 month before signing informed consent until 1 month after the last dose of the study drug, or are unable/unwilling to use effective contraception (including one or more non-pharmacological contraceptive methods or abstinence from heterosexual activity);
- At screening or within 4 weeks before screening, participants are in the acute phase of HIV-1 infection or have concurrent opportunistic infections or other serious AIDS-defining conditions;
- At screening or within 8 weeks before screening, resistance testing shows documented INSTI major resistance mutations, including but not limited to N155H and Q148H (as interpreted by the Stanford HIVdb database, including "low-level resistance [L]," "intermediate resistance [I]," and "high-level resistance [H]");
- At screening, the investigator determines the presence of uncontrolled clinically significant diseases (including cardiovascular, respiratory, digestive, endocrine/metabolic, neuropsychiatric, hematologic, or immune system disorders), such as resting systolic blood pressure ≥140 mmHg and/or diastolic blood pressure ≥90 mmHg, NYHA Class III or IV heart failure, etc.;
- At screening, ALT >5× upper limit of normal (ULN), or ALT >3×ULN with total bilirubin (TBIL) >1.5×ULN or direct bilirubin (DBIL) >ULN, or other laboratory abnormalities graded ≥3 per CTCAE v5.0;
- At screening, creatinine clearance <50 mL/min (calculated by Cockcroft-Gault formula);
- At screening, concurrent active hepatitis B virus (HBV) and/or hepatitis C virus (HCV) infection; or active syphilis infection requiring or having completed syphilis treatment <7 days prior (as judged by the investigator);
- Before screening, underwent major gastrointestinal surgery (except uncomplicated appendectomy or cholecystectomy), or the investigator judges that elective surgery may be required during the trial;
- Screening for the past 5 years, having suffered from malignant tumors (including cervical carcinoma in situ treated with cervical conization, or surgically cured basal cell carcinoma, squamous cell carcinoma, and/or carcinoma in situ [excluding Bowen's disease]);
- Known history of allergy to the investigational drug, chemically similar drugs, or excipients; or a history of allergic diseases requiring medication control (such as asthma, urticaria, atopic dermatitis [eczema], etc.) prior to screening.
- Within 5 years prior to screening, have a history of substance, alcohol, or other substance use disorders (excessive, inappropriate, or addictive use of substances, alcohol, or other substances for non-medical reasons, resulting in social, psychological, and physiological impairments).
- Use of any prohibited medication as specified in the protocol within 14 days before the first dose of the investigational drug;
- Before screening, intolerance to venipuncture, history of needle or blood phobia, or blood donation (including component donation) or significant blood loss (≥400 mL) or transfusion within 3 months before screening, or planned donation during the trial;
- Within 3 months prior to screening, have participated in any interventional clinical trials, including but not limited to drugs, vaccines, or medical devices (referring to subjects who have signed the informed consent form and received the investigational drug/device or placebo).
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Double
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
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Expérimental: ACC017 group
Participants receive ACC017 for the initial 2-week double-blind phase and continue to receive ACC017 in the subsequent open-label extension phase.
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ACC017
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Comparateur placebo: Placebo-ACC017 group
Participants receive matching placebo for the initial 2-week double-blind phase, and then switch to ACC017 in the subsequent open-label extension phase.
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Placebo
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Délai |
|---|---|
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To evaluate the percentage of participants achieving HIV-1 RNA <50 copies/mL at 16 weeks of treatment.
Délai: Week 16
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Week 16
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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To evaluate the change from baseline in HIV-1 RNA (log10 copies/mL) at 2 weeks of treatment;
Délai: Week 2
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Week 2
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To evaluate the time-course change in the percentage of participants achieving HIV-1 RNA <50 copies/mL during treatment
Délai: week 1 - week 16
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week 1 - week 16
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To evaluate the time-course change from baseline in HIV-1 RNA (log10 copies/mL) during treatment
Délai: week 1 - week 16
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week 1 - week 16
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To evaluate the change from baseline in CD4+ T-cell count at 16 weeks of treatment
Délai: week 16
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week 16
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To evaluate the time-course change from baseline in CD4+ T-cell count (cells/μL) during treatment
Délai: week 1 - week 16
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week 1 - week 16
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Incidence of Adverse Events (AEs)
Délai: week 1 - week 16
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Number and percentage of participants with treatment-emergent adverse events (TEAEs) during the study period.
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week 1 - week 16
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Participants with Clinically Significant Laboratory Test Abnormalities
Délai: week 1 - week 16
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Number of participants with clinically significant abnormalities in laboratory test results (including hematology and chemistry panels) during the study period.
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week 1 - week 16
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Participants with Clinically Significant Abnormal Vital Signs
Délai: week 1 - week 16
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Number of participants with clinically significant abnormalities in vital signs (including blood pressure, heart rate, respiratory rate, and body temperature) during the study period.
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week 1 - week 16
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Participants with Clinically Significant Abnormal Physical Examination Findings
Délai: week 1 - week 16
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Number of participants with clinically significant new or worsened abnormalities on physical examination during the study period.
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week 1 - week 16
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Participants with Clinically Significant Abnormal 12-Lead Electrocardiogram (ECG) Findings
Délai: week 1 - week 16
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Number of Participants with Clinically Significant QT Interval Prolongation on 12-Lead ECG
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week 1 - week 16
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Autres mesures de résultats
Mesure des résultats |
Délai |
|---|---|
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To evaluate the trough concentration (Ctrough) of ACC017 in blood during treatment
Délai: week 1 -week 16
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week 1 -week 16
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To evaluate genotypic resistance evolution from baseline in participants with virologic breakthrough (≥1 log10 copies/mL increase from nadir, or rebound to ≥400 copies/mL after suppression to <50 copies/mL) or meeting other resistance testing criteria.
Délai: week 1 - week 16
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week 1 - week 16
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To evaluate the change from baseline in genotypic resistance (non-nucleoside reverse transcriptase inhibitors(NNRTI), nucleoside reverse transcriptase inhibitors(NRTI), and integrase strand transfer inhibitors(INSTI)) at 16 weeks of treatment
Délai: week 16
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week 16
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Collaborateurs et enquêteurs
Les enquêteurs
- Chercheur principal: Zhang R Fang, Shanghai Clinical Center for Public Health
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
- Infections transmissibles par le sang
- Maladies urogénitales
- Maladies génitales
- Maladies du système immunitaire
- Infections par virus à ARN
- Maladies virales
- Maladies transmissibles
- Maladies sexuellement transmissibles, virales
- Maladies sexuellement transmissibles
- Infections à lentivirus
- Infections à rétroviridae
- Syndromes d'immunodéficience
- Maladies à virus lents
- Infections à VIH
- Syndrome immunodéficitaire acquis
- Infections
Autres numéros d'identification d'étude
- ADYY-ACC017-202
Informations sur les médicaments et les dispositifs, documents d'étude
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