A Clinical Study Evaluating the Safety, Tolerability, and Effect on HIV Reservoir of Ibalizumab Combined With Chidamide (a Histone Deacetylase Inhibitor) in People Living With HIV
HIV viral reservoirs represent the major barrier to curing AIDS, and effectively reducing viral reservoirs in people living with HIV through different strategies has become a research priority in the HIV field.
Ipilimumab-tovorafenib monoclonal antibody injection (Aituo combination antibody, QL1706) contains two engineered monoclonal antibodies targeting PD-1 and CTLA-4. Chidamide is the first independently developed histone deacetylase inhibitor in China. This study aims to evaluate the safety and efficacy of Aituo combination antibody combined with chidamide in people living with HIV.
This study adopts a modified "1+3+3" dose-escalation design. Initially, one participant will be enrolled at dose level 1 (DL1) for safety observation. If the treatment is well tolerated, the study will proceed to a standard 3+3 design, with sequential dose escalation to DL2 and DL3.
Three dose levels are planned: DL1, the starting dose, consists of ipilimumab-tovorafenib monoclonal antibody injection at 0.3 mg/kg once every 4 weeks ± 1 day for a total of three doses, in combination with chidamide 10 mg orally twice weekly for 12 weeks. DL2 consists of ipilimumab-tovorafenib monoclonal antibody injection at 1 mg/kg once every 4 weeks ± 1 day for a total of three doses, in combination with chidamide 10 mg orally twice weekly for 12 weeks. DL3 consists of ipilimumab-tovorafenib monoclonal antibody injection at 2 mg/kg once every 4 weeks ± 1 day for a total of three doses, in combination with chidamide 10 mg orally twice weekly for 12 weeks.
During dose escalation, progression to the next dose level or discontinuation of escalation will be determined according to the occurrence of dose-limiting toxicities (DLTs). The DLT observation window is 28 days after the first dose. Participants evaluable for DLT are those who complete the observation window or experience a DLT. After completion of dose escalation, the maximum tolerated dose (MTD) will be determined based on safety and tolerability. If the MTD is not reached, DL3 will be selected as the dose for subsequent study.
After determination of the MTD or the subsequent study dose, an additional 11 participants will be enrolled at that dose level to further evaluate safety, tolerability, and preliminary efficacy. The maximum total sample size of the study will be 29 participants.
A tanulmány áttekintése
Állapot
Körülmények
Beavatkozás / kezelés
Tanulmány típusa
Beiratkozás (Becsült)
Fázis
- 1. fázis
Részvételi kritériumok
Jogosultsági kritériumok
Tanulmányozható életkorok
- Felnőtt
- Idősebb felnőtt
Egészséges önkénteseket fogad
Leírás
Inclusion Criteria:
- Subjects aged 18-65 years.
- Confirmed HIV infection by both initial screening assay and Western blot (WB) confirmatory test.
- Receiving a stable ART regimen for at least 6 months.
- Viral load below the lower limit of detection.
- CD4+ T-cell count >200 cells/mm³.
- Voluntarily signed the informed consent form and able to comply with regular follow-up visits, specimen collection, and monitoring/treatment of study-related adverse events.
- Use effective contraception from 4 weeks prior to study initiation until 4 weeks after study completion.
Exclusion Criteria:
- Pregnant or breastfeeding women, or women planning to become pregnant during the study observation period.
- Subjects with poor treatment adherence.
- Receipt of immunosuppressants, other immunomodulatory agents, or cytotoxic drugs within 6 months prior to screening.
- Presence of severe underlying cardiac, cerebral, hepatic, renal, or other systemic diseases; neutrophil count <1000/mm³; platelet count <75,000/mm³; allergy to the investigational drug; or other contraindications to treatment.
- Presence of progressive (or active) malignancy, including but not limited to advanced, metastatic, or unresectable solid tumors or hematologic malignancies.
- Unwillingness to sign the informed consent form.
Tanulási terv
Hogyan készül a tanulmány?
Tervezési részletek
- Elsődleges cél: Kezelés
- Kiosztás: N/A
- Beavatkozó modell: Egyetlen csoportos hozzárendelés
- Maszkolás: Nincs (Open Label)
Fegyverek és beavatkozások
Résztvevő csoport / kar |
Beavatkozás / kezelés |
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Kísérleti: Ibalizumab Combined with Chidamide
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Three dose levels are planned: DL1, the starting dose, consists of ipilimumab-tovorafenib monoclonal antibody injection at 0.3 mg/kg once every 4 weeks ± 1 day for a total of three doses, in combination with chidamide 10 mg orally twice weekly for 12 weeks.
DL2 consists of ipilimumab-tovorafenib monoclonal antibody injection at 1 mg/kg once every 4 weeks ± 1 day for a total of three doses, in combination with chidamide 10 mg orally twice weekly for 12 weeks.
DL3 consists of ipilimumab-tovorafenib monoclonal antibody injection at 2 mg/kg once every 4 weeks ± 1 day for a total of three doses, in combination with chidamide 10 mg orally twice weekly for 12 weeks.
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Mit mér a tanulmány?
Elsődleges eredményintézkedések
Eredménymérő |
Intézkedés leírása |
Időkeret |
|---|---|---|
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Number and proportion of participants with treatment-emergent adverse events as assessed by CTCAE v5.0
Időkeret: A total of 8 study visits are planned, including Visit 1 (Week -2), Visit 2 (Week 0), Visit 3 (Week 4 ± 1 day), Visit 4 (Week 8 ± 1 day), Visit 5 (Week 12 ± 1 day), Visit 6 (Week 16 ± 1 day), Visit 7 (Week 20 ± 1 day), and Visit 8 (Week 24 ± 1 day).
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Safety will be assessed by the incidence, severity, seriousness, and relationship to study treatment of treatment-emergent adverse events, including adverse events, serious adverse events, laboratory abnormalities, vital sign abnormalities, and physical examination findings.
Adverse events will be graded according to CTCAE v5.0.
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A total of 8 study visits are planned, including Visit 1 (Week -2), Visit 2 (Week 0), Visit 3 (Week 4 ± 1 day), Visit 4 (Week 8 ± 1 day), Visit 5 (Week 12 ± 1 day), Visit 6 (Week 16 ± 1 day), Visit 7 (Week 20 ± 1 day), and Visit 8 (Week 24 ± 1 day).
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Number and proportion of participants who discontinue or interrupt study treatment due to adverse events
Időkeret: A total of 8 study visits are planned, including Visit 1 (Week -2), Visit 2 (Week 0), Visit 3 (Week 4 ± 1 day), Visit 4 (Week 8 ± 1 day), Visit 5 (Week 12 ± 1 day), Visit 6 (Week 16 ± 1 day), Visit 7 (Week 20 ± 1 day), and Visit 8 (Week 24 ± 1 day).
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Tolerability will be assessed by the number and proportion of participants who discontinue, interrupt, or modify study treatment because of adverse events or clinically significant laboratory abnormalities.
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A total of 8 study visits are planned, including Visit 1 (Week -2), Visit 2 (Week 0), Visit 3 (Week 4 ± 1 day), Visit 4 (Week 8 ± 1 day), Visit 5 (Week 12 ± 1 day), Visit 6 (Week 16 ± 1 day), Visit 7 (Week 20 ± 1 day), and Visit 8 (Week 24 ± 1 day).
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Másodlagos eredményintézkedések
Eredménymérő |
Intézkedés leírása |
Időkeret |
|---|---|---|
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Change from baseline in HIV reservoir size as measured by total HIV DNA and CA HIV RNA
Időkeret: A total of 8 study visits are planned, including Visit 1 (Week -2), Visit 2 (Week 0), Visit 3 (Week 4 ± 1 day), Visit 4 (Week 8 ± 1 day), Visit 5 (Week 12 ± 1 day), Visit 6 (Week 16 ± 1 day), Visit 7 (Week 20 ± 1 day), and Visit 8 (Week 24 ± 1 day).
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Exploratory efficacy will be assessed by the change from baseline in HIV reservoir size, measured by total HIV DNA and CA HIV RNA in peripheral blood mononuclear cells at scheduled study visits.
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A total of 8 study visits are planned, including Visit 1 (Week -2), Visit 2 (Week 0), Visit 3 (Week 4 ± 1 day), Visit 4 (Week 8 ± 1 day), Visit 5 (Week 12 ± 1 day), Visit 6 (Week 16 ± 1 day), Visit 7 (Week 20 ± 1 day), and Visit 8 (Week 24 ± 1 day).
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Együttműködők és nyomozók
Tanulmányi rekorddátumok
Tanulmány főbb dátumok
Tanulmány kezdete (Becsült)
Elsődleges befejezés (Becsült)
A tanulmány befejezése (Becsült)
Tanulmányi regisztráció dátumai
Először benyújtva
Először nyújtották be, amely megfelel a minőségbiztosítási kritériumoknak
Első közzététel (Tényleges)
Tanulmányi rekordok frissítései
Utolsó frissítés közzétéve (Tényleges)
Az utolsó frissítés elküldve, amely megfelel a minőségbiztosítási kritériumoknak
Utolsó ellenőrzés
Több információ
A tanulmányhoz kapcsolódó kifejezések
További vonatkozó MeSH feltételek
- Vérrel terjedő fertőzések
- Urogenitális betegségek
- Nemi szervek betegségei
- Immunrendszeri betegségek
- Fertőzések
- RNS vírusfertőzések
- Vírusos betegségek
- Fertőző betegségek
- Szexuális úton terjedő betegségek, vírusos
- Szexuális úton terjedő betegségek
- Lentivírus fertőzések
- Retroviridae fertőzések
- Immunhiányos szindrómák
- Lassú vírusos betegségek
- HIV fertőzések
- Szerzett immunhiányos szindróma
- N- (2-amino-5-fluor-benzil) -4- (N- (piridin-3-akril)-aminometil)-benzamid
Egyéb vizsgálati azonosító számok
- HCIT-003
Terv az egyéni résztvevői adatokhoz (IPD)
Tervezi megosztani az egyéni résztvevői adatokat (IPD)?
IPD terv leírása
Participant Privacy and Confidentiality:
Although data would be de-identified prior to sharing, the IPD encompass detailed clinical, virologic, and immunologic parameters. Given the specific sensitivities associated with the HIV-infected population and the nature of the medical information, a residual risk of re-identification through the triangulation of indirect identifiers persists. Public sharing of IPD may therefore contravene data protection regulations and the privacy assurances stipulated in the participant informed consent documentation.
- Limitations of Informed Consent Scope:
The informed consent form executed for this study does not explicitly authorize the disclosure of participant-level raw data to third parties or its deposition in public data repositories. The investigators are bound by legal and ethical obligations to utilize the data solely within the parameters approved in the study protocol and the corresponding informed consent.
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