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SA030 Injection in Healthy Participants

9 de noviembre de 2026 actualizado por: Suzhou Siran Biotechnology Co.,Ltd.

A Phase 1, Randomized, Double-blind, Placebo-controlled, Single-dose Escalation Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Immunogenicity of SA030 Injection in Healthy Participants

This is a randomized, double-blind, placebo-controlled study designed to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and immunogenicity of single ascending doses of SA030 injection in healthy participants. The planned dose levels include 100 mg, 200 mg, and 400 mg, with 8 eligible participants enrolled in each dose group.

All participants receive a single administration of the study drug on Day 1 (D1). In each dose group, the first 2 participants are enrolled as sentinel participants and randomized at a 1:1 ratio to receive either SA030 injection or placebo. After a 5-day safety observation period and favorable safety assessment by the investigator, the remaining 6 participants in the group will be enrolled and randomized at a 5:1 ratio to receive SA030 injection or placebo.

For dose escalation, at least 6 out of 8 participants in each dose group must complete the 14-day safety observation period (up to Day 15 [D15]). Subsequent dose escalation to the next higher dose level can only be initiated after safety review and approval by the Safety Review Committee (SRC).

Descripción general del estudio

Tipo de estudio

Intervencionista

Inscripción (Estimado)

24

Fase

  • Fase 1

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

Ubicaciones de estudio

    • Jilin
      • Changchun, Jilin, Porcelana, 130000
        • The First Bethune Hospital of Jilin University
        • Contacto:

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

18 años a 55 años (Adulto)

Acepta Voluntarios Saludables

Sí

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  • Participants aged 18 to 55 years, with a BMI of 25-40 kg/m².
  • Healthy participants as determined by medical history, physical examination, vital signs, ECG and laboratory assessments.
  • Willing to use effective contraception and have no pregnancy plans from screening to 6 months after study drug administration and/or throughout the study, with no intent to donate sperm or ova.

Exclusion Criteria:

  • Medical history:

    • Nervous, cardiovascular, hematologic/lymphatic, immune, gastrointestinal, renal, respiratory, endocrine disorders, history of malignancy, or psychiatric/psychological conditions
    • Has hypertension at screening (blood pressure ≥150/95 mmHg), diabetes mellitus (FPG ≥7.0 mmol/L and/or HbA1c ≥7.0%), hyperlipidemia (LDL-C ≥4.9 mmol/L or TG ≥500 mg/dL (5.65 mmol/L)), or gout.
    • Has a history of bleeding disorders, recent active bleeding, or clinically significant bleeding risk; or has coagulation abnormalities deemed clinically significant by the Investigator at screening.
    • Tests positive for HBV, HCV, HIV, or syphilis (positive Treponema pallidum, excluding those with negative RPR).
    • Has undergone major surgery within 6 months prior to screening, or plans to undergo surgery during the study period.
    • Has severe infection or trauma within 4 weeks prior to screening.
    • Has clinically significant hepatic space-occupying lesions, gallbladder lesions, pancreatic or renal abnormalities identified on abdominal ultrasound at screening.
    • Has severe allergic diathesis.
    • Has prior severe intolerance to subcutaneous injection.
    • Has skin abnormalities at injection sites.
    • Has risk factors for TdP, requires concurrent use of QT/QTc-prolonging / TdP-inducing drugs, or has high-risk bundle branch block.
  • Has clinically significant laboratory abnormalities at screening as judged by the Investigator.

  • concomitant medications:

    • Has received live attenuated vaccine within 1 month prior to screening, or plans to receive live attenuated vaccine during the study period.
    • Has used any prescription drugs, herbal medicines, or over-the-counter medications within 14 days prior to administration of the investigational product.
    • Has used any over-the-counter medications, herbal medicines or dietary supplements that may significantly affect body weight or metabolism within 1 month prior to screening.
    • Has participated in another drug clinical trial within 3 months prior to treatment in this study or within 5 half-lives of the other investigational product ; or has prior use of siRNA or antisense oligonucleotide drugs within 6 months prior to administration of the study drug.
  • Other

    • Has non-physiological blood loss ≥ 400 mL within 1 month prior to screening (including trauma, blood sampling, blood donation), or plans to donate blood during the study or within 30 days after study drug administration.
    • Has weekly alcohol intake >14 units within 3 months prior to screening ; or has a positive alcohol breath test on the day before dosing ; or is unable to abstain from alcohol during the in-hospital study period.
    • Has current or history of illicit drug use/substance abuse, or tests positive on urine drug screen on the day prior to dosing.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Cuadruplicar

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: SA030 Injection, 100 mg

Single subcutaneous injection of SA030 at 100 mg dose, one-time administration.

Single subcutaneous injection of SA030 injection at a dose of 100 mg, one-time administration on Day 1.

Experimental: SA030 Injection, 200mg

Single subcutaneous injection or SA030 at 200 mg dose, one-time administration.

Single subcutaneous injection of SA030 injection at a dose of 200 mg, one-time administration on Day 1.

Experimental: SA030 Injection, 400mg

Single subcutaneous injection or SA030 at 400 mg dose, one-time administration.

Single subcutaneous injection of SA030 injection at a dose of 400 mg, one-time administration on Day 1.

Comparador de placebos: placebo

Single subcutaneous injection of placebo, one-time administration.

Single subcutaneous injection of placebo, one-time administration.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Periodo de tiempo
Number of participants with adverse events (AEs) and serious adverse events (SAEs)
Periodo de tiempo: Approximatly 9 months
Approximatly 9 months
Number of participants with clinically significant laboratory abnormalities
Periodo de tiempo: Approximatly 9 months
Approximatly 9 months

Medidas de resultado secundarias

Medida de resultado
Periodo de tiempo
Peak plasma concentration (Cmax)
Periodo de tiempo: Pre-dose, multiple timepoints post-dose up to D15
Pre-dose, multiple timepoints post-dose up to D15
Time to peak plasma concentration (Tmax)
Periodo de tiempo: Pre-dose, multiple timepoints post-dose up to D15
Pre-dose, multiple timepoints post-dose up to D15
Plasma concentration-time curve from time zero to the time of the last quantifiable concentration (AUC0-t)
Periodo de tiempo: Pre-dose, multiple timepoints post-dose up to D15
Pre-dose, multiple timepoints post-dose up to D15
Elimination half-life (t1/2)
Periodo de tiempo: Pre-dose, multiple timepoints post-dose up to D15
Pre-dose, multiple timepoints post-dose up to D15
Changes in BMI
Periodo de tiempo: baseline, up to 9 months
baseline, up to 9 months
Changes in body fat content
Periodo de tiempo: baseline, up to 9 months
baseline, up to 9 months
Changes in hepatic fat content
Periodo de tiempo: baseline, up to 9 months
baseline, up to 9 months
Changes in ALK7 expression
Periodo de tiempo: baseline, up to 9 months
baseline, up to 9 months
Number of participants with anti-SA030 antibodies (immunogenicity)
Periodo de tiempo: baseline, up to 9 months
baseline, up to 9 months
Change in QTcF relative to baseline and relative to placebo compared to baseline
Periodo de tiempo: Pre-dose, multiple timepoints post-dose up to Day 5
Pre-dose, multiple timepoints post-dose up to Day 5

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

16 de octubre de 2026

Finalización primaria (Estimado)

31 de octubre de 2027

Finalización del estudio (Estimado)

31 de octubre de 2027

Fechas de registro del estudio

Enviado por primera vez

8 de octubre de 2026

Primero enviado que cumplió con los criterios de control de calidad

9 de noviembre de 2026

Publicado por primera vez (Actual)

13 de noviembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

13 de noviembre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

9 de noviembre de 2026

Última verificación

1 de octubre de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • SAOB101-CN

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

INDECISO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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