- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07606950
Phase III Study of HRS-5635 in Nucleos(t)Ide Analogue-suppressed HBeAg-negative Patients With Chronic Hepatitis B
23. juli 2026 oppdatert av: Fujian Shengdi Pharmaceutical Co., Ltd.
A Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-designed Phase III Clinical Study to Evaluate the Efficacy and Safety of HRS-5635 Injection in Nucleos(t)Ide Analogue-suppressed HBeAg-negative Patients With Chronic Hepatitis B
This study is intended to confirm the efficacy, safety, pharmacokinetic (PK) profile, and immunogenicity of HRS-5635 injection as compared to the placebo arm in nucleos(t)ide analogue-suppressed HBeAg-negative patients with chronic hepatitis B. The total duration of the study, including screening (up to 4 weeks), the double-blind treatment stage (60 weeks),NAs-only treatment stage(12 weeks) and the off-treatment follow-up (24 weeks), is up to approximately 100 weeks at maximum for each participant.
Studieoversikt
Status
Rekruttering
Intervensjon / Behandling
Studietype
Intervensjonell
Registrering (Antatt)
540
Fase
- Fase 3
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiekontakt
- Navn: Xiaopeng Wang
- Telefonnummer: 0518-82342973
- E-post: xiaopeng.wang@hengrui.com
Studiesteder
-
-
Guangzhou
-
Guangzhou, Guangzhou, Kina, 510515
- Rekruttering
- Nanfang Hospital, Southern Medical University
-
Hovedetterforsker:
- Jinlin Hou
-
-
Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Voksen
- Eldre voksen
Tar imot friske frivillige
Nei
Beskrivelse
Inclusion Criteria:
- Chronic hepatitis B defined as HBV infection documented for at least 6 months prior to screening;
- Virologically suppressed on nucleoside or nucleotide analogues treatment with HBV DNA below the lower limit of quantitation;
- HBeAg negative at screening;
- On commercially available NAs monotherapy for at least 24 weeks before randomization, and the dosing regimen remained unchanged for at least 4 weeks before randomization;
- Need to take effective contraceptive measures;
- Volunteer to sign an informed consent.
Exclusion Criteria:
- History of cirrhosis or clinical evidence of hepatic decompensation, confirmed or suspected liver cancer, with other liver diseases other than chronic hepatitis B that may affect the evaluation of the study;
- With autoimmune disease;
- History of solid organ transplantation or hematopoietic stem cell transplantation;
- Clinically significant and unstable or uncontrolled severe cardiovascular and cerebrovascular diseases;
- Malignant tumors were diagnosed within 5 years prior to randomization;
- Major trauma or major surgery within the 12 weeks prior to randomization, or surgical plans or other treatment during the study period which the investigators determined may influence the evaluation of the study results;
- Laboratory tests during the screening period were obviously abnormal;
- Prolonged ECG QTcF or other clinically significant abnormal results that may pose a significant safety risk to the subject during the screening period;
- History of drug use, alcohol or drug abuse in the 12 months prior to randomization;
- Participated in clinical study of other drugs (received experimental drugs);
- Pregnant or nursing women;
- Allergic to a drug ingredient or component;
- Other reasons for ineligibility as judged by the investigators.
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Firemannsrom
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Placebo komparator: Placebo
|
Placebo, administered by subcutaneous injection.
|
|
Eksperimentell: HRS-5635 Injection
|
HRS-5635 Injection, administered by subcutaneous injection;
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Percentage of participants with sustained HBV DNA suppression and HBsAg loss within 24 weeks after discontinuation of all HBV therapy
Tidsramme: 24 weeks after discontinuation of all CHB treatment
|
24 weeks after discontinuation of all CHB treatment
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Percentage of participants with sustained HBV DNA suppression and HBsAg < 100 IU/mL
Tidsramme: Pre-specified time points up to 24 weeks after discontinuation of all CHB treatment
|
Pre-specified time points up to 24 weeks after discontinuation of all CHB treatment
|
|
Percentage of participants with sustained HBV DNA suppression and HBsAg < 10 IU/mL
Tidsramme: Pre-specified time points up to 24 weeks after discontinuation of all CHB treatment
|
Pre-specified time points up to 24 weeks after discontinuation of all CHB treatment
|
|
Percentage of participants with sustained HBV DNA suppression
Tidsramme: Pre-specified time points up to 24 weeks after discontinuation of all CHB treatment
|
Pre-specified time points up to 24 weeks after discontinuation of all CHB treatment
|
|
Percentage of participants with HBsAg < 100 IU/mL
Tidsramme: Pre-specified time points up to 24 weeks after discontinuation of all CHB treatment
|
Pre-specified time points up to 24 weeks after discontinuation of all CHB treatment
|
|
Percentage of participants with HBsAg < 10 IU/mL
Tidsramme: Pre-specified time points up to 24 weeks after discontinuation of all CHB treatment
|
Pre-specified time points up to 24 weeks after discontinuation of all CHB treatment
|
|
Changes from baseline in mean log10 HBsAg levels
Tidsramme: Pre-specified time points up to 24 weeks after discontinuation of all CHB treatment
|
Pre-specified time points up to 24 weeks after discontinuation of all CHB treatment
|
|
Percentage of participants with HBsAg loss
Tidsramme: Pre-specified time points up to 24 weeks after discontinuation of all CHB treatment
|
Pre-specified time points up to 24 weeks after discontinuation of all CHB treatment
|
|
Percentage of participants with HBsAg seroconversion
Tidsramme: Pre-specified time points up to 24 weeks after discontinuation of all CHB treatment
|
Pre-specified time points up to 24 weeks after discontinuation of all CHB treatment
|
|
Percentage of participants with HBeAb positive
Tidsramme: Pre-specified time points up to 24 weeks after discontinuation of all CHB treatment
|
Pre-specified time points up to 24 weeks after discontinuation of all CHB treatment
|
|
Percentage of participants with virologic breakthrough
Tidsramme: Pre-specified time points up to 24 weeks after discontinuation of all CHB treatment
|
Pre-specified time points up to 24 weeks after discontinuation of all CHB treatment
|
|
Percentage of participants with drug resistance
Tidsramme: Pre-specified time points up to 24 weeks after discontinuation of all CHB treatment
|
Pre-specified time points up to 24 weeks after discontinuation of all CHB treatment
|
|
Relapse rate after discontinuation of NAs therapy
Tidsramme: Up to 24 weeks after discontinuation of NAs treatment
|
Up to 24 weeks after discontinuation of NAs treatment
|
|
Treatment-emergent adverse events
Tidsramme: Up to 24 weeks after discontinuation of NAs treatment
|
Up to 24 weeks after discontinuation of NAs treatment
|
|
Percentage of participants with detectable anti-drug antibodies
Tidsramme: Pre-specified time points up to 24 weeks after discontinuation of all CHB treatment
|
Pre-specified time points up to 24 weeks after discontinuation of all CHB treatment
|
|
Percentage of participants who meet the criteria for stopping nucleos(t)ide analogue (NA) therapy
Tidsramme: Week 72 and Week 96
|
Week 72 and Week 96
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart (Faktiske)
17. juli 2026
Primær fullføring (Antatt)
1. juni 2028
Studiet fullført (Antatt)
1. juni 2028
Datoer for studieregistrering
Først innsendt
19. mai 2026
Først innsendt som oppfylte QC-kriteriene
19. mai 2026
Først lagt ut (Faktiske)
26. mai 2026
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
24. juli 2026
Siste oppdatering sendt inn som oppfylte QC-kriteriene
23. juli 2026
Sist bekreftet
1. mars 2026
Mer informasjon
Begreper knyttet til denne studien
Andre studie-ID-numre
- HRS-5635-301
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
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