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A First-in-human Study to Investigate Single Doses of DCY636 in Healthy Volunteers and Multiple Doses in Participants With Moderate to Severe Atopic Dermatitis

18. august 2026 oppdatert av: Novartis Pharmaceuticals

A Two-part, Randomized, Participant- and Investigator-blinded, Placebo Controlled First-in-human Study to Investigate the Safety, Tolerability and Pharmacokinetics of DCY636 in a Single Ascending Dose Part in Healthy Participants and in a Multiple Dose Part in Participants With Moderate to Severe Atopic Dermatitis

The purpose of this first-in-human (FIH) study is to assess the safety and tolerability, pharmacokinetics (PK), immunogenicity (IG) and pharmacodynamics (PD) of DCY636. The results are intended to support the further clinical development of DCY636 in future studies.

Studieoversikt

Status

Rekruttering

Detaljert beskrivelse

This is a two-part FIH, randomized, placebo-controlled, participant- and investigator-blinded study in healthy participants (Part 1) and participants with moderate to severe AD (Part 2).

Studietype

Intervensjonell

Registrering (Antatt)

63

Fase

  • Fase 1

Kontakter og plasseringer

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

Studiekontakt

  • Navn: Novartis Pharmaceuticals

Studer Kontakt Backup

Studiesteder

      • Fukuoka, Japan, 812-0025
        • Rekruttering
        • Novartis Investigative Site

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

Tar imot friske frivillige

Ja

Beskrivelse

Key Inclusion Criteria:

Healthy Participants (Part 1)

• Healthy male and non-childbearing potential female participants 18 to 55 years of age inclusive.

Participants with moderate to severe atopic dermatitis (Part 2)

  • Males and non-pregnant females age 18 years or older
  • Diagnosis of atopic dermatitis for at least 1 year not adequately controlled by topicals
  • Moderate to severe atopic dermatitis as defined by all of the following:

    • EASI score ≥12 at screening visit and ≥16 at baseline (BL) visit
    • IGA score ≥3 at screening visit and baseline visit
    • Total Body surface area (BSA) affected by AD ≥ 10 % at screening visit and baseline visit
    • Peak Pruritus NRS score ≥4 at baseline visit, based on weekly average of daily assessment in the week prior to baseline visit

Key Exclusion Criteria:

All Participants (Part 1, Part 2)

  • Use of other investigational drugs within the last 30 days or 5 half-lives of the other drugs prior to initial dosing, whichever is longer.
  • Meet any of the prohibited medication use criteria at baseline visit.
  • A positive syphilis test result during screening period.
  • Evidence of active or latent TB infection, as determined by T-Spot test during screening period.
  • History of immunodeficiency diseases, or a positive human immunodeficiency virus (HIV) test result.
  • Recent (within last half year) or ongoing helminth infection.
  • History of hepatitis B or hepatitis C or serologic evidence for viral hepatitis. A positive Hepatitis B virus surface antigen (HBsAg), Hepatitis B virus core antibody (HBcAb) and/or Hepatitis B surface antibody (HBsAb) test during screening period excludes a participant. A positive test for HBsAb can be included if the test for HBsAg and HBcAb are negative and the history of hepatitis B vaccination is known. Participants with a positive Hepatitis C virus (HCV) antibody test should be excluded.

Healthy Participants (Part 1)

  • Women of childbearing potential
  • Smokers Participants with moderate to severe atopic dermatitis (Part 2)
  • Regular use (more than 2 visits per week) of a tanning booth/parlor or extended sun exposure (per investigator judgement) within 4 weeks prior to baseline visit
  • Have any chronic, uncontrolled medical condition, which would put the participant at increased risk during study participation, such as uncontrolled: diabetes, hypertension, morbid obesity, thyroid, adrenal, cardiovascular, pulmonary, hepatic, renal, neurologic or psychiatric disease, or other disease of concern, as per investigator judgment
  • Women of childbearing potential (WOCBP) are excluded unless they are using highly effective methods of contraception (failure rate < 1% per year) while taking study treatment and for 202 days (= 5 times the terminal half-life) of study treatment after stopping study treatment.

Other protocol-defined inclusion/exclusion criteria may apply.

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: Dobbelt

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Part 1- Cohort A1: Dose Level 1 DCY636
Cohort A1: Dose Level 1 DCY636 in healthy participants.
Participants will receive DCY636
Eksperimentell: Part 1- Cohort A2: Dose Level 2 DCY636
Cohort A2: Dose Level 2 DCY636 in healthy participants.
Participants will receive DCY636
Eksperimentell: Part 1- Cohort A3: Dose Level 3 DCY636
Cohort A3: Dose Level 3 DCY636 in healthy participants.
Participants will receive DCY636
Eksperimentell: Part 1- Cohort A4: Dose Level 4 DCY636
Cohort A4: Dose Level 4 DCY636 in healthy participants.
Participants will receive DCY636
Eksperimentell: Part 1- Cohort B1: Dose Level 5 DCY636
Cohort B1: Dose Level 5 DCY636 in healthy participants.
Participants will receive DCY636
Eksperimentell: Part 1- Cohort B2: Dose Level 6 DCY636
Cohort B2: Dose Level 6 DCY636 in healthy participants.
Participants will receive DCY636
Eksperimentell: Part 2- Cohort C1: Dose Level 7 DCY636
Part 2- Cohort C1: Dose Level 7 DCY636 in participants with moderate to severe atopic dermatitis.
Participants will receive DCY636
Placebo komparator: Part 1- Cohort A1: Placebo
Cohort A1: Placebo in healthy participants.
Deltakerne vil motta Placebo
Placebo komparator: Part 1- Cohort A2: Placebo
Cohort A2: Placebo in healthy participants.
Deltakerne vil motta Placebo
Placebo komparator: Part 1- Cohort A3: Placebo
Cohort A3: Placebo in healthy participants.
Deltakerne vil motta Placebo
Placebo komparator: Part 1- Cohort A4: Placebo
Cohort A4: Placebo in healthy participants.
Deltakerne vil motta Placebo
Placebo komparator: Part 1- Cohort B1: Placebo
Cohort B1: Placebo in healthy participants.
Deltakerne vil motta Placebo
Placebo komparator: Part 1- Cohort B2: Placebo
Cohort B2: Placebo in healthy participants.
Deltakerne vil motta Placebo
Placebo komparator: Part 2- Cohort C1: Placebo
Part 2- Cohort C1: Placebo in participants with moderate to severe atopic dermatitis.
Deltakerne vil motta Placebo

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Part 1-Incidence of adverse events (AEs) and serious adverse events (SAEs)
Tidsramme: Up to approximately 202 days
Number of participants with adverse events (AEs) and serious adverse events (SAEs), including changes in vital signs, electrocardiograms (ECGs) and laboratory values qualifying and reported as AEs.
Up to approximately 202 days
Part 2-Incidence of adverse events (AEs) and serious adverse events (SAEs)
Tidsramme: Up to approximately 301 days
Number of participants with adverse events (AEs) and serious adverse events (SAEs), including changes in vital signs, electrocardiograms (ECGs) and laboratory values qualifying and reported as AEs.
Up to approximately 301 days

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Part 1-Pharmacokinetic (PK) parameter: Cmax of DCY636
Tidsramme: up to Day 202
Cmax is the maximum (peak) observed blood concentration of DCY636 after dose administration.
up to Day 202
Part 1-Pharmacokinetic (PK) parameter: AUC of DCY636
Tidsramme: up to Day 202
AUC is the area under the plasma concentration-time curve.
up to Day 202
Part 1-Anti-drug antibodies against DCY636
Tidsramme: up to Day 202
To assess immunogenicity (IG) of DCY636.
up to Day 202
Part 2-Pharmacokinetic (PK) parameter: Cmax of DCY636
Tidsramme: up to Day 301
Cmax is the maximum (peak) observed blood concentration of DCY636 after dose administration.
up to Day 301
Part 2-Pharmacokinetic (PK) parameter: AUC of DCY636
Tidsramme: up to Day 301
AUC is the area under the plasma concentration-time curve.
up to Day 301
Part 2-Anti-drug antibodies against DCY636
Tidsramme: up to Day 301
To assess immunogenicity (IG) of DCY636.
up to Day 301

Samarbeidspartnere og etterforskere

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

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)

2. juni 2026

Primær fullføring (Antatt)

27. januar 2028

Studiet fullført (Antatt)

28. januar 2028

Datoer for studieregistrering

Først innsendt

18. mai 2026

Først innsendt som oppfylte QC-kriteriene

18. mai 2026

Først lagt ut (Faktiske)

22. mai 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

19. august 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

18. august 2026

Sist bekreftet

1. august 2026

Mer informasjon

Begreper knyttet til denne studien

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

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