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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 opdateret af: 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.

Studieoversigt

Status

Rekruttering

Betingelser

Intervention / Behandling

Detaljeret 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).

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

63

Fase

  • Fase 1

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

  • Navn: Novartis Pharmaceuticals

Undersøgelse Kontakt Backup

Studiesteder

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

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Voksen

Tager imod sunde 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

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Dobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Part 1- Cohort A1: Dose Level 1 DCY636
Cohort A1: Dose Level 1 DCY636 in healthy participants.
Participants will receive DCY636
Eksperimentel: Part 1- Cohort A2: Dose Level 2 DCY636
Cohort A2: Dose Level 2 DCY636 in healthy participants.
Participants will receive DCY636
Eksperimentel: Part 1- Cohort A3: Dose Level 3 DCY636
Cohort A3: Dose Level 3 DCY636 in healthy participants.
Participants will receive DCY636
Eksperimentel: Part 1- Cohort A4: Dose Level 4 DCY636
Cohort A4: Dose Level 4 DCY636 in healthy participants.
Participants will receive DCY636
Eksperimentel: Part 1- Cohort B1: Dose Level 5 DCY636
Cohort B1: Dose Level 5 DCY636 in healthy participants.
Participants will receive DCY636
Eksperimentel: Part 1- Cohort B2: Dose Level 6 DCY636
Cohort B2: Dose Level 6 DCY636 in healthy participants.
Participants will receive DCY636
Eksperimentel: 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.
Deltagerne vil modtage Placebo
Placebo komparator: Part 1- Cohort A2: Placebo
Cohort A2: Placebo in healthy participants.
Deltagerne vil modtage Placebo
Placebo komparator: Part 1- Cohort A3: Placebo
Cohort A3: Placebo in healthy participants.
Deltagerne vil modtage Placebo
Placebo komparator: Part 1- Cohort A4: Placebo
Cohort A4: Placebo in healthy participants.
Deltagerne vil modtage Placebo
Placebo komparator: Part 1- Cohort B1: Placebo
Cohort B1: Placebo in healthy participants.
Deltagerne vil modtage Placebo
Placebo komparator: Part 1- Cohort B2: Placebo
Cohort B2: Placebo in healthy participants.
Deltagerne vil modtage Placebo
Placebo komparator: Part 2- Cohort C1: Placebo
Part 2- Cohort C1: Placebo in participants with moderate to severe atopic dermatitis.
Deltagerne vil modtage Placebo

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
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
Foranstaltningsbeskrivelse
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

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

2. juni 2026

Primær færdiggørelse (Anslået)

27. januar 2028

Studieafslutning (Anslået)

28. januar 2028

Datoer for studieregistrering

Først indsendt

18. maj 2026

Først indsendt, der opfyldte QC-kriterier

18. maj 2026

Først opslået (Faktiske)

22. maj 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

19. august 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

18. august 2026

Sidst verificeret

1. august 2026

Mere information

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