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A Phase 1 Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of SRSD107 in Healthy Chinese Subjects

15. juni 2026 oppdatert av: Sirius Therapeutics Co., Ltd.

A Phase 1, Randomized, Double-blind, Placebo-controlled, Single Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Subcutaneously Administered SRSD107 in Healthy Subjects

This was a Phase 1, randomized, double-blind, placebo-controlled, single ascending dose study to evaluate the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of subcutaneously administered SRSD107 in Chinese healthy subjects. SRSD107 is a synthetic, chemically modified double-stranded siRNA designed to silence hepatic FXI mRNA, thereby modulating coagulation.

Studieoversikt

Status

Fullført

Forhold

Studietype

Intervensjonell

Registrering (Faktiske)

48

Fase

  • Fase 1

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • Beijing Municipality
      • Beijing, Beijing Municipality, Kina
        • Beijing Tiantan Hospital affiliated to Capital Medical University

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

Ja

Beskrivelse

Inclusion Criteria:

  • Males or females, of any race, between 18 and 65 years of age, inclusive.
  • Body mass index between 18.0 and 32.0 kg/square meter, inclusive.
  • In good health, determined by no clinically significant findings from medical history, physical examination, clinical laboratory evaluations, 12 lead ECG, and vital signs measurements, at screening and check in, as assessed by the investigator (or designee).
  • Activated partial thromboplastin time and prothrombin time within the normal reference range.
  • Females will not be pregnant or lactating, and females of childbearing potential and males will agree to use contraception as pre-defined in the protocol.
  • Able to comprehend and willing to sign an ICF and to abide by the study restrictions.

Exclusion Criteria:

  • Significant history or clinical manifestation of any metabolic, allergic, dermatological, hepatic, renal, hematological, pulmonary, cardiovascular, gastrointestinal, neurological, respiratory, endocrine, or psychiatric disorder, as determined by the investigator (or designee).
  • History or evidence of any abnormal bleeding or coagulation disorder; or evidence of coagulopathy, prolonged or unexplained, clinically significant bleeding, or frequent unexplained bruising or thrombus formation; or a history of spontaneous bleeding.
  • Evidence of an active or suspected cancer, or a history of malignancy, within 5 years prior to screening. Nonmelanoma skin cancer, curatively treated localized prostate cancer, or other carcinoma in situ are not exclusionary, providing that they did not require systemic therapy and are considered cured.
  • Acute of febrile illness within 7 days prior to dose administration or evidence of active infection.
  • Any major surgery within 3 months prior to screening or plan to have any surgery during the study.
  • History of clinically significant hypersensitivity, intolerance, or allergy to any drug compound, oligonucleotide, GalNAc, food, or other substance, as determined by the investigator (or designee).
  • Systolic blood pressure >140 mmHg or <90 mmHg, or diastolic blood pressure >90 mmHg or <50 mmHg confirmed by repeat measurement.
  • QT interval corrected for heart rate using Fridericia's method (QTcF) >450 ms confirmed by repeat measurement.
  • Platelet count or hemoglobin level below the lower limit of normal.
  • Alanine aminotransferase, aspartate aminotransferase, gamma glutamyl transferase, alkaline phosphatase, or total bilirubin >1.5 × the upper limit of normal.
  • Estimated glomerular filtration rate <80 mL/min/1.73 square meter, as calculated by the 2021 Chronic Kidney Disease Epidemiology Collaboration equation.
  • Positive hepatitis B and C, positive human immunodeficiency virus test or positive syphilis test. Subjects whose results are compatible with prior immunization may be included.
  • Positive pregnancy test at screening or check in.
  • Women who are menstruating at dosing, and women whose past volume of menstrual fluid was >80 mL or menstrual periods were >7 days.
  • Use or intend to use any of the following, as determined by the investigator (or designee): 1) prescription medications/products or herbal products within 14 days or 5 terminal elimination half lives, whichever is longer, prior to dose administration in this study; 2) over the counter medications/products within 7 days prior to dose administration in this study. Recommended doses of vitamin and mineral supplements, over the counter analgesics (eg, paracetamol or ibuprofen for the treatment of acute conditions [eg, headache]), prescription oral, implantable, transdermal, injectable, or intrauterine contraceptives, and other products that have been approved by the investigator will not be exclusionary. Hormone replacement therapy will not be exclusionary, providing that the regimen has been stable for at least 2 months prior to screening and will not be changed during the study.
  • Immunization with any live vaccine within 6 weeks prior to screening, or expected to require immunization with any live vaccine during the study.
  • Receipt of an investigational drug in the past 90 days or 5 half lives of that drug, whichever is longer, prior to dosing in this study.
  • Receipt of any siRNA treatment within 12 months or any antisense oligonucleotide treatment within 6 months prior to dosing in this study.
  • Have previously completed or withdrawn from this study or any other study investigating SRSD107 and have previously received SRSD107.
  • Drug abuse or addiction within 1 year prior to screening, as determined by the investigator (or designee).
  • Positive alcohol or cotinine test result or positive urine drug screen (confirmed by repeat) at screening or check in.
  • Regular alcohol consumption of >21 units per week for males and >14 units for females within 12 months prior to screening. One unit of alcohol equals 375 mL of beer or lager (3.5%), 100 mL of wine (13.5%), or 30 mL of spirits (40%).
  • Use of tobacco or nicotine containing products within 1 months prior to screening.
  • Receipt of blood products within 3 months prior to check in.
  • Loss of >500 mL whole blood or donation of >200 mL blood products within 1 month prior to screening.
  • History of intolerance to subcutaneous injections, or scarring (eg, from surgical procedures or burns) in areas when subcutaneous dose administration may occur.
  • Poor peripheral venous access.
  • Subjects who, in the opinion of the investigator (or designee), should not participate in this study.

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
Sodium chloride for subcutaneous injection.
Eksperimentell: SRSD107
SRSD107 is a synthetic, chemically modified double-stranded siRNA designed to silence hepatic FXI mRNA, thereby modulating coagulation.

Hva måler studien?

Primære resultatmål

Resultatmål
Tidsramme
Proportion of adverse events (AEs)
Tidsramme: up to 168 days post last dose
up to 168 days post last dose
Proportion of Serious Adverse Events (SAEs)
Tidsramme: up to 168 days post last dose
up to 168 days post last dose

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Peak Concentration
Tidsramme: Day 1 to Day 3
Day 1 to Day 3
Time to maximum concentration
Tidsramme: Day1 to Day3
Day1 to Day3
Elimination half-life
Tidsramme: Day1 to Day3
Day1 to Day3
Area Under Curve
Tidsramme: Day1 to Day3
Day1 to Day3
Apparent total clearance
Tidsramme: Day1 to Day3
Day1 to Day3
Prothrombin Time
Tidsramme: up to 168 days post last dose
up to 168 days post last dose
Activated Partial Thromboplastin Time
Tidsramme: up to 168 days post last dose
up to 168 days post last dose
FXI avtivity in peripheral blood (quantitative laboratory measurement)
Tidsramme: up to 168 days post last dose
Coagulation Factor XI (FXI) is a plasma serine protease zymogen predominantly synthesized in the liver. As a key protein in the intrinsic coagulation pathway, it circulates in the bloodstream as a homodimer.
up to 168 days post last dose
FXI antigen concentration in peripheral blood (quantitative laboratory measurement)
Tidsramme: up to 168 days post last dose
Coagulation Factor XI (FXI) is a plasma serine protease zymogen predominantly synthesized in the liver. As a key protein in the intrinsic coagulation pathway, it circulates in the bloodstream as a homodimer.
up to 168 days post last dose

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Studieleder: Qiuyue Qu, Sirius Therapeutics Co., Ltd.

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)

29. mars 2024

Primær fullføring (Faktiske)

2. mars 2025

Studiet fullført (Faktiske)

2. mars 2025

Datoer for studieregistrering

Først innsendt

8. juni 2026

Først innsendt som oppfylte QC-kriteriene

15. juni 2026

Først lagt ut (Faktiske)

17. juni 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

17. juni 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

15. juni 2026

Sist bekreftet

1. juni 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • SRSD107-102
  • ChiCTR2600120343 (Registeridentifikator: Chinese Clinical Trial Registry (ChiCTR))

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

produkt produsert i og eksportert fra USA

Nei

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