- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07580924
A Study of NHL907 in Healthy Adult Participants
8 juin 2026 mis à jour par: NeuHyll AUS Pty Ltd
A Randomized, Double-Blind, Placebo-Controlled, Multiple Ascending Dose Study to Assess Safety, Tolerability, and Pharmacokinetics of NHL907 Combination Drug Following Multiple Oral Doses in Healthy Adult Participants
The goal of this study is to evaluate the safety, tolerability and pharmacokinetics of NHL907 when administered as multiple oral doses in healthy adult participants.
Aperçu de l'étude
Statut
Recrutement
Les conditions
Intervention / Traitement
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
- Nom: James Connell, MD
- Numéro de téléphone: +61 (0)8 7088 7900
- E-mail: james.connell@cmax.com.au
Lieux d'étude
-
-
South Australia
-
Adelaide, South Australia, Australie, 5000
- Recrutement
- CMAX Clinical Research Pty Ltd
-
Contact:
- James Connell, MD
- Numéro de téléphone: +61 (0)8 7088 7900
- E-mail: cmax@cmax.com.au
-
-
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
- Adulte
Accepte les volontaires sains
Oui
La description
Inclusion Criteria:
- Healthy adult male and female participants aged between 18 and 60 years of age, inclusive.
- Has a body mass index (BMI) between ≥ 18 and ≤ 32 kg/m2 inclusive, with body weight ≥ 50 kg at Screening.
- Able and willing to understand and sign the informed consent form, communicate meaningfully with study personnel, and comply with all study restrictions, procedures, laboratory tests, and other study requirements.
- In good health, determined by the Investigator on the basis of medical history, physical examination, vital signs, Screening laboratory results, Screening ECG, and mental status.
- Participants of non-childbearing potential should be congenitally or surgically sterile or in a menopausal state as confirmed by follicle-stimulating hormone (FSH) concentrations (≥ 40 IU/L at Screening).
- Female participants with childbearing potential must agree to use accepted contraceptive regimens from time of Screening, during the study, and for at least 60 days after end of study.
- Male participants with the potential to father a child must agree to abstain from sperm donation and to use accepted contraceptive regimens from Screening, during the study, and for at least 90 days after end of study.
- Participants should agree to refrain from donating blood for at least 30 days after end of study.
Exclusion Criteria:
If an individual meets any of the following criteria, they will be ineligible for this study:
- History or evidence of clinically significant disorders and deemed not suitable to participants in the study by the Principal Investigator or delegate.
- History or presence of any gastrointestinal (GI) disease (except for Gilbert's syndrome or cholecystectomy) or condition that could compromise the participant safety and/or absorption of the study drug, including irritable bowel disease, known untreated helicobacter pylori infection, abnormal gastric emptying, dyspepsia, GI ulcers, GI bleeding, or GI surgeries within 6 months before Screening.
- Have a known hypersensitivity to any component of the IP formulation or related derivatives of each component.
- Have abnormalities in resting vital signs at Screening, on Day -1, or on Day 1 prior to dosing.
- History of or ongoing cardiac abnormalities as assessed during Screening, including abnormal and clinically relevant ECG changes, considered by the Investigator.
- History of smoking in the past 90 days before Screening which is defined as more than the equivalent of 5 cigarettes weekly (including alternative nicotine products such as cigars, e-cigarettes, chewing tobacco, etc.); and /or have a positive urine test for cotinine at Screening or Baseline, or unable to abstain from smoking starting from at least 3 days before Screening, or Day -1 / check-in until end of study.
- History of illicit or prescription drug abuse or addiction within 1 year of Screening, or positive urine drug screen at Screening or Baseline. Participants who used a THC / CBD product within 30 days before Screening and added a deterrent from any use before that are excluded.
- History of alcohol abuse (unless fully recovered with no use of alcohol within the 12 months prior to Screening), which is defined as exceeding an average weekly intake of 21 standard drinks for males or 14 standard drinks for females (1 standard drink is equivalent to 5 ounces [150 mL] of wine or 12 ounces [360 mL] of beer or 1.5 ounces [45 mL] of hard liquor); or positive alcohol breath test at Screening or Baseline; incapable to refrain from consuming alcohol starting from at least 48 h prior to Day 1 / check-in until end of study.
- Has participated in any interventional trial or drug investigation or device investigation (including placebo) within 30 days, or 5 half-lives of the IP, whichever is longer, prior to Screening or has the intention to participate in another trial during the present study.
- Have received vaccines within 14 days and within 60 days for live-attenuated vaccines before screening.
- Have any medical condition(s) screened by the Investigator and determined to be ineligible or have any acute illness within 7 days prior to Day 1 will be excluded or may be considered for the next cohort if still within their screening window.
- Have clinical safety laboratory parameters at Screening (serum chemistry and lipid panel, hematology, coagulation, and urinalysis) that are outside the normal limits and are considered clinically significant in the opinion of the Investigator and the Sponsor's MM (e.g., LFTs / bilirubin ≥ 1.5 ULN and eGFR ≤ 60 ml/min/1.73 m2). Participants with elevated unconjugated bilirubin (Gilbert's syndrome) are not excluded.
- History of suicidal ideations or suicide attempts, including current instances of either case or any "yes" response to C-SSRS at screening.
- The participant is pregnant, lactating, or planning to become pregnant within 6 months of being discharged from the trial.
- Use of any prescription medicine within 2 weeks, or over the counter (OTC) medicine, herbal remedy, or nutritional supplement, or within 5 half-lives of any drugs, whichever is longer prior to dosing, except for vitamins and occasional use of paracetamol / acetaminophen (≤ 2 g/day; no more than 3 consecutive days) which will be reviewed by the PI and the Sponsor's MM for determination of acceptability.
- Have undergone surgery within 90 days before Screening, or have surgery planned during the study period or within 90 days after the last dose or has previously undergone any surgery that may affect drug absorption, distribution, metabolism, or excretion during the study.
- Blood donation or loss of ≥ 450 mL of blood within 90 days before dosing or receiving a blood transfusion within 90 days before dosing. Platelet/Plasma donation is prohibited within 30 days before Screening and until at least 30 days after study completion.
- Positive hepatitis B virus (HBsAg), hepatitis B core antibody (HBcAb), hepatitis C virus (HCV-Ab), human immunodeficiency virus (HIV-1 and HIV-2), or syphilis at Screening.
- History of malignancy, with the exception of non-melanoma skin cancer or curatively treated cancer that has not been in full remission for ≥ 5 years, without evidence of recurrence.
- Have any special dietary requirements that may include CYP2D6 inhibitors, e.g., grapefruit, bitter citrus products, tonic water, or any other requirement that would prevent compliance with study standardized meals.
- History of dysphagia or difficulty swallowing tablets / capsules.
- Unable or unwilling to comply with the lifestyle guidelines and evaluations detailed in this protocol, for the duration of the study or have a situation or condition that, in the opinion of the Investigator, may interfere with participation in the study.
- Participants who cannot perform venous blood sampling (i.e., poor venous access or vasovagal response to injection).
- Any other circumstances or laboratory abnormalities that, in the Investigator's judgement, may result in an unacceptable increase in risk to the participant, or impair the participant's ability to participate in and complete the study, or could preclude the evaluation of the participant's response.
- Have any clinically significant abnormality on physical examination at Screening, on Day -1, or on Day 1 prior to dosing which in the opinion of the Investigator would exclude them from the study.
- History of a severe allergic reaction to any drug or multiple food / drug allergies.
- Heavy caffeine drinker (> 5 cups or glasses of caffeinated beverages, e.g., coffee, tea, cola per day).
- Have any condition which, in the judgement of the Investigator, would prevent the participant from completing the study or complying with study procedures and requirements.
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 séquentielle
- Masquage: Tripler
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: NHL907 Dose 1
|
Investigational product NHL907
|
|
Expérimental: NHL907 Dose 2
|
Investigational product NHL907
|
|
Expérimental: NHL907 Dose 3
|
Investigational product NHL907
|
|
Expérimental: NHL907 Dose 4
|
Investigational product NHL907
|
|
Expérimental: NHL907 Dose 5
|
Investigational product NHL907
|
|
Expérimental: NHL907 Dose 6
|
Investigational product NHL907
|
|
Expérimental: NHL907 Dose 7
|
Investigational product NHL907
|
|
Expérimental: NHL907 Dose 8
|
Investigational product NHL907
|
|
Comparateur placebo: Placebo Dose 1
Placebo for Dose 1
|
NHL907 matching placebo
|
|
Comparateur placebo: Placebo Dose 2
Placebo for Dose 2
|
NHL907 matching placebo
|
|
Comparateur placebo: Placebo Dose 3
Placebo for Dose 3
|
NHL907 matching placebo
|
|
Comparateur placebo: Placebo Dose 4
Placebo for Dose 4
|
NHL907 matching placebo
|
|
Comparateur placebo: Placebo Dose 5
Placebo for Dose 5
|
NHL907 matching placebo
|
|
Comparateur placebo: Placebo Dose 6
Placebo for Dose 6
|
NHL907 matching placebo
|
|
Comparateur placebo: Placebo Dose 7
Placebo for Dose 7
|
NHL907 matching placebo
|
|
Comparateur placebo: Placebo Dose 8
Placebo for Dose 8
|
NHL907 matching placebo
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Délai |
|---|---|
|
Number of Participants with Treatment Emergent Adverse Events
Délai: Baseline to 7 days after the last dose (Day 14)
|
Baseline to 7 days after the last dose (Day 14)
|
Mesures de résultats secondaires
Mesure des résultats |
Délai |
|---|---|
|
Cmax: Maximum observed plasma concentration
Délai: Day 1, Day 7
|
Day 1, Day 7
|
|
Tmax: Time of occurrence of Cmax
Délai: Day 1, Day 7
|
Day 1, Day 7
|
|
AUC0-24: Area under the concentration-time curve from 0 to 24 hours
Délai: Day 1, Day 7
|
Day 1, Day 7
|
|
AUC0-inf: Area under the concentration-time curve from 0 to infinity
Délai: Day 1, Day 7
|
Day 1, Day 7
|
|
Cmax/dose: Cmax normalized by dose
Délai: Day 1, Day 7
|
Day 1, Day 7
|
|
CL/F: Apparent total clearance
Délai: Day 1, Day 7
|
Day 1, Day 7
|
|
Vz/F: Apparent volume of distribution
Délai: Day 1, Day 7
|
Day 1, Day 7
|
|
AUC0-24/dose: AUC0-24 normalized by dose
Délai: Day 1, Day 7
|
Day 1, Day 7
|
|
AUC0-inf/dose: AUC0-inf normalized by dose
Délai: Day 1, Day 7
|
Day 1, Day 7
|
|
t1/2: Apparent terminal elimination half-life
Délai: Day 1, Day 7
|
Day 1, Day 7
|
|
Ctrough: Trough plasma concentration
Délai: Day 4-7
|
Day 4-7
|
|
RA Cmax: Observed accumulation ratio based on Cmax
Délai: Day 7 to Day 1
|
Day 7 to Day 1
|
Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Parrainer
Collaborateurs
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 (Réel)
12 mai 2026
Achèvement primaire (Estimé)
1 février 2027
Achèvement de l'étude (Estimé)
1 avril 2027
Dates d'inscription aux études
Première soumission
29 avril 2026
Première soumission répondant aux critères de contrôle qualité
5 mai 2026
Première publication (Réel)
12 mai 2026
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
10 juin 2026
Dernière mise à jour soumise répondant aux critères de contrôle qualité
8 juin 2026
Dernière vérification
1 juin 2026
Plus d'information
Termes liés à cette étude
Autres numéros d'identification d'étude
- NHL907-101
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
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 .