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A Study of NHL907 in Healthy Adult Participants

5. Mai 2026 aktualisiert von: 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.

Studienübersicht

Status

Noch keine Rekrutierung

Studientyp

Interventionell

Einschreibung (Geschätzt)

64

Phase

  • Phase 1

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

Studienorte

    • South Australia
      • Adelaide, South Australia, Australien, 5000
        • CMAX Clinical Research Pty Ltd
        • Kontakt:

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Erwachsene

Akzeptiert gesunde Freiwillige

Ja

Beschreibung

Inclusion Criteria:

  1. Healthy adult male and female participants aged between 18 and 60 years of age, inclusive.
  2. Has a body mass index (BMI) between ≥ 18 and ≤ 32 kg/m2 inclusive, with body weight ≥ 50 kg at Screening.
  3. 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.
  4. 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.
  5. 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).
  6. 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.
  7. 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.
  8. 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:

  1. History or evidence of clinically significant disorders and deemed not suitable to participants in the study by the Principal Investigator or delegate.
  2. 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.
  3. Have a known hypersensitivity to any component of the IP formulation or related derivatives of each component.
  4. Have abnormalities in resting vital signs at Screening, on Day -1, or on Day 1 prior to dosing.
  5. History of or ongoing cardiac abnormalities as assessed during Screening, including abnormal and clinically relevant ECG changes, considered by the Investigator.
  6. 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.
  7. 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.
  8. 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.
  9. 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.
  10. Have received vaccines within 14 days and within 60 days for live-attenuated vaccines before screening.
  11. 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.
  12. 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.
  13. History of suicidal ideations or suicide attempts, including current instances of either case or any "yes" response to C-SSRS at screening.
  14. The participant is pregnant, lactating, or planning to become pregnant within 6 months of being discharged from the trial.
  15. 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.
  16. 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.
  17. 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.
  18. 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.
  19. 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.
  20. 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.
  21. History of dysphagia or difficulty swallowing tablets / capsules.
  22. 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.
  23. Participants who cannot perform venous blood sampling (i.e., poor venous access or vasovagal response to injection).
  24. 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.
  25. 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.
  26. History of a severe allergic reaction to any drug or multiple food / drug allergies.
  27. Heavy caffeine drinker (> 5 cups or glasses of caffeinated beverages, e.g., coffee, tea, cola per day).
  28. 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.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: Zufällig
  • Interventionsmodell: Sequenzielle Zuweisung
  • Maskierung: Verdreifachen

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: NHL907 Dose 1
Investigational product NHL907
Experimental: NHL907 Dose 2
Investigational product NHL907
Experimental: NHL907 Dose 3
Investigational product NHL907
Experimental: NHL907 Dose 4
Investigational product NHL907
Experimental: NHL907 Dose 5
Investigational product NHL907
Experimental: NHL907 Dose 6
Investigational product NHL907
Experimental: NHL907 Dose 7
Investigational product NHL907
Experimental: NHL907 Dose 8
Investigational product NHL907
Placebo-Komparator: Placebo Dose 1
Placebo for Dose 1
NHL907 matching placebo
Placebo-Komparator: Placebo Dose 2
Placebo for Dose 2
NHL907 matching placebo
Placebo-Komparator: Placebo Dose 3
Placebo for Dose 3
NHL907 matching placebo
Placebo-Komparator: Placebo Dose 4
Placebo for Dose 4
NHL907 matching placebo
Placebo-Komparator: Placebo Dose 5
Placebo for Dose 5
NHL907 matching placebo
Placebo-Komparator: Placebo Dose 6
Placebo for Dose 6
NHL907 matching placebo
Placebo-Komparator: Placebo Dose 7
Placebo for Dose 7
NHL907 matching placebo
Placebo-Komparator: Placebo Dose 8
Placebo for Dose 8
NHL907 matching placebo

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Zeitfenster
Number of Participants with Treatment Emergent Adverse Events
Zeitfenster: Baseline to 7 days after the last dose (Day 14)
Baseline to 7 days after the last dose (Day 14)

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Zeitfenster
Cmax: Maximum observed plasma concentration
Zeitfenster: Day 1, Day 7
Day 1, Day 7
Tmax: Time of occurrence of Cmax
Zeitfenster: Day 1, Day 7
Day 1, Day 7
AUC0-24: Area under the concentration-time curve from 0 to 24 hours
Zeitfenster: Day 1, Day 7
Day 1, Day 7
AUC0-inf: Area under the concentration-time curve from 0 to infinity
Zeitfenster: Day 1, Day 7
Day 1, Day 7
Cmax/dose: Cmax normalized by dose
Zeitfenster: Day 1, Day 7
Day 1, Day 7
CL/F: Apparent total clearance
Zeitfenster: Day 1, Day 7
Day 1, Day 7
Vz/F: Apparent volume of distribution
Zeitfenster: Day 1, Day 7
Day 1, Day 7
AUC0-24/dose: AUC0-24 normalized by dose
Zeitfenster: Day 1, Day 7
Day 1, Day 7
AUC0-inf/dose: AUC0-inf normalized by dose
Zeitfenster: Day 1, Day 7
Day 1, Day 7
t1/2: Apparent terminal elimination half-life
Zeitfenster: Day 1, Day 7
Day 1, Day 7
Ctrough: Trough plasma concentration
Zeitfenster: Day 4-7
Day 4-7
RA Cmax: Observed accumulation ratio based on Cmax
Zeitfenster: Day 7 to Day 1
Day 7 to Day 1

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

1. Mai 2026

Primärer Abschluss (Geschätzt)

1. Februar 2027

Studienabschluss (Geschätzt)

1. April 2027

Studienanmeldedaten

Zuerst eingereicht

29. April 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

5. Mai 2026

Zuerst gepostet (Tatsächlich)

12. Mai 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

12. Mai 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

5. Mai 2026

Zuletzt verifiziert

1. Mai 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Andere Studien-ID-Nummern

  • NHL907-101

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

NEIN

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .

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