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A Phase I Study of HLX109 in Healthy Participants

6 novembre 2026 mis à jour par: Shanghai Henlius Biotech

A Randomized, Double-Blind, Single Ascending Dose, Phase I Clinical Study to Evaluate Safety, Tolerability and Pharmacokinetic Profiles of HLX109 in Healthy Participants

This study is a randomized, double-Blind, single ascending dose, phase I clinical study to evaluate safety, tolerability and pharmacokinetic profiles of HLX109 in healthy participants

Aperçu de l'étude

Statut

Pas encore de recrutement

Les conditions

Intervention / Traitement

Description détaillée

This first-in-human clinical trial of HLX109 is a randomized, double-blind, placebo-controlled, single ascending dose phase Ia clinical study to evaluate the safety, tolerability, and pharmacokinetic characteristics of HLX109 in healthy adult participants. Each participant is expected to participate in the study for 112 days. The first 28 days constitute the screening period, followed by a study drug administration and an 84-day follow-up period.

Type d'étude

Interventionnel

Inscription (Estimé)

64

Phase

  • La phase 1

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Lieux d'étude

      • Melbourne, Australie
    • Anhui
      • Hefei, Anhui, Chine
        • The Second Affiliated Hospital of Anhui Medical University
        • Contact:

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

18 ans à 55 ans (Adulte)

Accepte les volontaires sains

Oui

Sexes éligibles pour l'étude

Tout

La description

Inclusion Criteria:

  1. Voluntarily participates in the clinical study, with a full understanding of the study procedures; provides written informed consent by signing and dating the informed consent form (ICF); and is willing and able to comply with all protocol-specified requirements and follow-up visits.
  2. Adult male or female, aged 18 (inclusive) to 55 years (inclusive) at the time of ICF signing.
  3. Body mass index (BMI) between 18.5 (inclusive) and 28.0 (exclusive) kg/m2 at screening.
  4. No clinically significant abnormalities in medical history or clinical evaluations (including physical examination, clinical laboratory assessments, diagnostic imaging, vital signs, and 12-lead ECG) at screening. At the investigator's discretion, screening assessments may be repeated to confirm eligibility, provided that all assessments are completed within the defined screening window.
  5. A female participant must be of no childbearing potential, postmenopausal, or premenopausal with one of the following records: hysterectomy, tubal ligation, or bilateral salpingectomy. The heterosexual partners of all participants and the participants must agree to take contraceptive measures during the treatment period and at least 3 months after the last dose of IMP. (Appendix 2.)
  6. Prior to randomization, complete all age-appropriate vaccinations according to current immunization guidelines.

Exclusion Criteria:

  1. Pregnant or lactating women.

  2. With sunburn, scar tissue, tattoos (more than 25% of body area), open sores, or branding at screening that, in the opinion of the investigator, would interfere with the assessment of adverse skin reactions.

  3. History of clinically significant hypersensitivity or allergic reactions to two or more medications, or known hypersensitivity to IMP or any of its excipients, or a history of anaphylaxis. Additionally, individuals with a history of multiple and/or severe allergic manifestations (including food allergies) are excluded. (Note: Prospective participants with seasonal allergic rhinitis/allergies are eligible for enrollment, provided they are currently asymptomatic or their symptoms are well-controlled).

  4. History of venous thromboembolic events and/or has a first-degree relative with an idiopathic venous thromboembolic event.

  5. History or evidence of substance or alcohol abuse, defined as follows:

    • A history of substance abuse within 1 year prior to screening, or a positive urine drug screen at the screening.
    • A history of alcohol abuse within 6 months prior to screening, or a positive breath alcohol test at the screening.
  6. History of the following diseases with a clear diagnosis within 6 months prior to screening: cardiovascular diseases, hematological diseases, respiratory diseases, gastrointestinal diseases, hepatic impairment, renal impairment (e.g. glomerular filtration rate less than 75 mL/min/1.73m²), endocrine, metabolic, neurological, psychiatric, dermatological, musculoskeletal, or immunological disorders. Participants will also be excluded if they present with any other concurrent medical condition that, in the judgment of the investigator, may confound the interpretation of the study data or compromise participant safety.

  7. History of hemorrhagic diathesis (including but not limited to non-traumatic bleeding) within 6 months before screening or diagnosed diseases that increase hemorrhagic diathesis.

  8. Malignancy or increased risk of malignancy prior to screening: suspected and/or diagnosed with any malignancy (except for basal cell carcinoma, squamous cell carcinoma of skin in situ, or cervical carcinoma in situ occurring within 5 years prior to screening with no evidence of recurrence after treatment).

  9. Major surgery (including procedures under general anesthesia) within 3 months prior to screening or organ transplantation prior to screening. Or still in the state of disease, trauma, or incomplete recovery after surgery at screening (significant changes in organ function, or significantly limited ability to live and work compared with that before disease, trauma, or surgery, or requiring continuous rehabilitation treatment), or planning to undergo surgery during the study.

  10. Chronic or recurrent infection at screening, systemic or local severe infection requiring hospitalization or intravenous injection of antibiotics within 1 month before screening, or history of acute infection within 14 days before screening.

  11. Any severe herpes infection at any time prior to before screening, but not limited to, disseminated herpes (ever), herpes encephalitis (ever), recurrent herpes zoster (defined as 2 episodes within 2 years prior to Screening), or ophthalmic herpes (ever).

  12. Any condition requires medication and/or other treatments at screening.

  13. Evidence of active or prior tuberculosis (TB) infection on lung imaging during the screening period.

  14. Abnormalities in 12-lead ECG at screening or admission, such as corrected QT (QTc) interval > 450 ms in males and > 470 ms in females (Fridericia's method).

  15. Abnormal results of the following Laboratory assessments at screening or admission:

    • Hemoglobin > 1.1 × upper limit of normal (ULN), or Hemoglobin < 0.9× lower limit of normal (LLN)
    • Platelet count > 1.1 ×ULN, or Platelet count < 0.9× LLN
    • Neutrophil count < 1.5 × 109/L.
    • Alkaline phosphatase (ALP) > 1.5 × ULN, or total bilirubin (TBIL) > 1.5 × ULN, or alanine aminotransferase (ALT) > 1.5 × ULN, or aspartate aminotransferase (AST) > 1.5 × ULN, or AST/ALT between 1-1.5 × ULN (inclusive) and considered clinically significant by the investigator, or blood amylase > 1 × ULN.
    • International normalized ratio (INR) > 1.5.
    • Blood thyroid-stimulating hormone (TSH) < 1×LLN, or TSH > 1 ×ULN.
    • Estimated glomerular filtration rate (eGFR) < 75mL/min/1.73 m2, or urine protein qualitative≥2+
    • Positive interferon-γ release assay.
    • Positive serology for Human Immunodeficiency Virus (HIV) antibody, Hepatitis B Virus surface antigen (HBsAg), or Hepatitis C Virus (HCV) antibody; or a positive treponemal test for syphilis.
  16. Have participated in a clinical study of other investigational products before screening, with an interval between this study and the previous study being too short: within 1 month before the first dose of this study or within 5 half-lives of the previous investigational product (whichever is longer). Or plan to participate in clinical studies of other investigational products before completing all scheduled assessments in this clinical study. Participants who violate the restrictions on concomitant medications (Appendix 6) should be excluded.

  17. Have participated in surgical or device clinical studies within 3 months prior to screening, or are currently participating in other surgical or device clinical studies, or plan to participate in other surgical or device clinical studies during this study.

  18. Receipt of any vaccine within 14 days prior to randomization or planned receipt of any vaccine during the study.

  19. Unable to follow the lifestyle restrictions (Appendix 3) during the study.

  20. Prescription and over the counter (OTC) drugs, herbal medicines, vitamins, minerals, or oral iron supplements (Appendix 3) not approved by the investigator during the study.

  21. Unable or unwilling to undergo repeated venipuncture due to poor tolerance or difficulty in finding a vein, or with a history of fear of blood or needles.

  22. Donated whole blood or blood components (more than 400 mL) or lost a large amount of blood (more than 400 mL) within 2 months prior to IMP administration , or plan to donate whole blood or blood components during the study.

  23. The participant has a hierarchical or dependent relationship with the investigator or the study site (including employees and their immediate family members), or has any other condition that, as determined by the investigator, renders the participants unsuitable for participation or places their rights and well-being at risk.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Tripler

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: HLX109

Dose Escalation

HLX109: A mg, SC, single dose

HLX109: B mg, SC, single dose

HLX109: C mg, SC, single dose

HLX109: D mg, SC, single dose

HLX109: E mg, SC, single dose

HLX109: F mg, SC, single dose

HLX109: G mg, SC, single dose

Comparateur placebo: Placebo

Dose Escalation

Placebo: A mg, SC, single dose

HLX109: B mg, SC, single dose

HLX109: C mg, SC, single dose

HLX109: D mg, SC, single dose

HLX109: E mg, SC, single dose

HLX109: F mg, SC, single dose

HLX109: G mg, SC, single dose

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Safety: number and percentage of participants with adverse events (AEs) assessed by CTCAE v6.0
Délai: Up to approximately 84 days
Up to approximately 84 days
Safety: number and percentage of participants with serious adverse events (SAEs) assessed by CTCAE v6.0
Délai: Up to approximately 84 days
Up to approximately 84 days
Safety: number and percentage of participants with adverse events of special interest (AESIs) assessed by CTCAE v6.0
Délai: Up to approximately 84 days
Up to approximately 84 days
Safety: number and percentage of participants with laboratory abnormalities
Délai: Up to approximately 84 days

Following parameters were analyzed for laboratory examination: hematology (hemoglobin, hematocrit, red blood cell count, platelet count, white blood cell count, total neutrophils, eosinophils, monocytes, basophils, lymphocytes); chemistry (blood urea nitrogen, creatinine, glucose, calcium, sodium, potassium, chloride, total bicarbonate, aspartate aminotransferase, alanine aminotransferase, total bilirubin, alkaline phosphatase, uric acid, albumin, total protein); urinalysis (decimal logarithm of reciprocal of hydrogen ion activity [pH], glucose, protein, blood, ketones, nitrites, leukocyte esterase, microscopy[if urine tested positive for blood, protein, nitrites or leukocyte esterase]. Laboratory abnormalities were assessed based on values outside the reference range and/or judged clinically significant by the investigator according to NCI CTCAE Version 6.0.

Up to approximately 84 days
Safety: number and percentage of participants with notable 12-Lead electrocardiogram (ECG) values
Délai: Up to approximately 84 days

Criteria for notable ECG values were as follow: corrected QT interval by Fredericia formula (QTcF) in msec new(newly occurring post-baseline value) > 500, or increase from baseline >60.

Up to approximately 84 days
Safety: number and percentage of participants with clinically notable vital signs
Délai: Up to approximately 84 days

Criteria for notable vital signs: Pulse rate <40 beats per minute (bpm) to >120 bpm, Diastolic blood pressure < 50 millimeter of mercury (mmHg), systolic blood pressure < 90 mmHg.

Up to approximately 84 days

Mesures de résultats secondaires

Mesure des résultats
Délai
PK: peak concentration (Cmax)
Délai: Up to approximately 84 days
Up to approximately 84 days
PK: area under the concentration-time curve (AUC0-t, AUC0-inf)
Délai: Up to approximately 84 days
Up to approximately 84 days
PK: time to peak concentration (Tmax)
Délai: Up to approximately 84 days
Up to approximately 84 days
PK: terminal elimination half-life (t1/2)
Délai: Up to approximately 84 days
Up to approximately 84 days
PK: apparent clearance (CL/F)
Délai: Up to approximately 84 days
Up to approximately 84 days
PK: apparent volume of distribution (Vz/F)
Délai: Up to approximately 84 days
Up to approximately 84 days
PK: mean residence time (MRT)
Délai: Up to approximately 84 days
Up to approximately 84 days
PK: percentage of extrapolated AUC (%AUCex)
Délai: Up to approximately 84 days
Up to approximately 84 days
Immunogenicity: incidence of anti-drug antibody (ADA) against HLX109 and recombinant human hyaluronidase.
Délai: Up to approximately 84 days
Up to approximately 84 days
Immunogenicity: incidence of neutralizing antibody (NAb) against HLX109 and recombinant human hyaluronidase.
Délai: Up to approximately 84 days
Up to approximately 84 days
Exploratory: serum free/total soluble IL-1RAP (sIL-1RAP) levels
Délai: Up to approximately 84 days
Up to approximately 84 days
Exploratory: ex vivo stimulated cytokine release levels in whole peripheral blood
Délai: Up to approximately 84 days
Up to approximately 84 days
Exploratory: IL-1RAP receptor occupancy (RO)
Délai: Up to approximately 84 days
Up to approximately 84 days

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Parrainer

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

18 novembre 2026

Achèvement primaire (Estimé)

20 septembre 2027

Achèvement de l'étude (Estimé)

20 novembre 2027

Dates d'inscription aux études

Première soumission

18 octobre 2026

Première soumission répondant aux critères de contrôle qualité

6 novembre 2026

Première publication (Réel)

13 novembre 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

13 novembre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

6 novembre 2026

Dernière vérification

1 novembre 2026

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • HLX109-FIH101

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

produit fabriqué et exporté des États-Unis.

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .