A Phase 1 Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of SRSD107 in Healthy Chinese Subjects
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
Panoramica dello studio
Stato
Stato
Condizioni
Condizioni
Intervento / Trattamento
Intervento / Trattamento
Tipo di studio
Tipo di studio
Iscrizione (Effettivo)
Iscrizione
Fase
Fase
- Fase 1
Contatti e Sedi
Luoghi di studio
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Beijing Municipality
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Beijing, Beijing Municipality, Cina
- Beijing Tiantan Hospital affiliated to Capital Medical University
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Criteri di partecipazione
Criteri di ammissibilità
Criteri di ammissibilità
Età idonea allo studio
- Adulto
- Adulto più anziano
Accetta volontari sani
Descrizione
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.
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Quadruplicare
Numero di armi
Armi e interventi
Gruppo di partecipanti / ArmGruppo di partecipanti / Arm |
Intervento / TrattamentoIntervento / Trattamento |
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Comparatore placebo: Placebo
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Sodium chloride for subcutaneous injection.
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Sperimentale: SRSD107
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SRSD107 is a synthetic, chemically modified double-stranded siRNA designed to silence hepatic FXI mRNA, thereby modulating coagulation.
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misure di risultato primarie
Misura del risultato |
Lasso di tempo |
|---|---|
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Proportion of adverse events (AEs)
Lasso di tempo: up to 168 days post last dose
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up to 168 days post last dose
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Proportion of Serious Adverse Events (SAEs)
Lasso di tempo: up to 168 days post last dose
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up to 168 days post last dose
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Misure di risultato secondarie
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Peak Concentration
Lasso di tempo: Day 1 to Day 3
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Day 1 to Day 3
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Time to maximum concentration
Lasso di tempo: Day1 to Day3
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Day1 to Day3
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Elimination half-life
Lasso di tempo: Day1 to Day3
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Day1 to Day3
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Area Under Curve
Lasso di tempo: Day1 to Day3
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Day1 to Day3
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Apparent total clearance
Lasso di tempo: Day1 to Day3
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Day1 to Day3
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Prothrombin Time
Lasso di tempo: up to 168 days post last dose
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up to 168 days post last dose
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Activated Partial Thromboplastin Time
Lasso di tempo: up to 168 days post last dose
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up to 168 days post last dose
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FXI avtivity in peripheral blood (quantitative laboratory measurement)
Lasso di tempo: up to 168 days post last dose
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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.
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up to 168 days post last dose
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FXI antigen concentration in peripheral blood (quantitative laboratory measurement)
Lasso di tempo: up to 168 days post last dose
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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.
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up to 168 days post last dose
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Collaboratori e investigatori
Sponsor
Sponsor
Investigatori
Investigatori
- Direttore dello studio: Qiuyue Qu, Sirius Therapeutics Co., Ltd.
Studiare le date dei record
Studia le date principali
Inizio studio (Effettivo)
Inizio studio
Completamento primario (Effettivo)
Completamento primario
Completamento dello studio (Effettivo)
Completamento dello studio
Date di iscrizione allo studio
Primo inviato
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Primo Inserito
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento pubblicato
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
Altri numeri di identificazione dello studio
- SRSD107-102
- ChiCTR2600120343 (Identificatore di registro: Chinese Clinical Trial Registry (ChiCTR))
Piano per i dati dei singoli partecipanti (IPD)
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