- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT07604324
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
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
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
Studientyp
Einschreibung (Geschätzt)
Phase
- Phase 1
Kontakte und Standorte
Studienkontakt
- Name: Novartis Pharmaceuticals
Studieren Sie die Kontaktsicherung
- Name: Novartis Pharmaceuticals
- Telefonnummer: +81337978748
- E-Mail: novartis.email@novartis.com
Studienorte
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Fukuoka, Japan, 812-0025
- Rekrutierung
- Novartis Investigative Site
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Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
Akzeptiert gesunde Freiwillige
Beschreibung
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.
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Doppelt
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
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Experimental: Part 1- Cohort A1: Dose Level 1 DCY636
Cohort A1: Dose Level 1 DCY636 in healthy participants.
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Participants will receive DCY636
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Experimental: Part 1- Cohort A2: Dose Level 2 DCY636
Cohort A2: Dose Level 2 DCY636 in healthy participants.
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Participants will receive DCY636
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Experimental: Part 1- Cohort A3: Dose Level 3 DCY636
Cohort A3: Dose Level 3 DCY636 in healthy participants.
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Participants will receive DCY636
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Experimental: Part 1- Cohort A4: Dose Level 4 DCY636
Cohort A4: Dose Level 4 DCY636 in healthy participants.
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Participants will receive DCY636
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Experimental: Part 1- Cohort B1: Dose Level 5 DCY636
Cohort B1: Dose Level 5 DCY636 in healthy participants.
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Participants will receive DCY636
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Experimental: Part 1- Cohort B2: Dose Level 6 DCY636
Cohort B2: Dose Level 6 DCY636 in healthy participants.
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Participants will receive DCY636
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Experimental: Part 2- Cohort C1: Dose Level 7 DCY636
Part 2- Cohort C1: Dose Level 7 DCY636 in participants with moderate to severe atopic dermatitis.
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Participants will receive DCY636
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Placebo-Komparator: Part 1- Cohort A1: Placebo
Cohort A1: Placebo in healthy participants.
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Teilnehmer erhalten Placebo
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Placebo-Komparator: Part 1- Cohort A2: Placebo
Cohort A2: Placebo in healthy participants.
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Teilnehmer erhalten Placebo
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Placebo-Komparator: Part 1- Cohort A3: Placebo
Cohort A3: Placebo in healthy participants.
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Teilnehmer erhalten Placebo
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Placebo-Komparator: Part 1- Cohort A4: Placebo
Cohort A4: Placebo in healthy participants.
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Teilnehmer erhalten Placebo
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Placebo-Komparator: Part 1- Cohort B1: Placebo
Cohort B1: Placebo in healthy participants.
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Teilnehmer erhalten Placebo
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Placebo-Komparator: Part 1- Cohort B2: Placebo
Cohort B2: Placebo in healthy participants.
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Teilnehmer erhalten Placebo
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Placebo-Komparator: Part 2- Cohort C1: Placebo
Part 2- Cohort C1: Placebo in participants with moderate to severe atopic dermatitis.
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Teilnehmer erhalten Placebo
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Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Part 1-Incidence of adverse events (AEs) and serious adverse events (SAEs)
Zeitfenster: Up to approximately 202 days
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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.
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Up to approximately 202 days
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Part 2-Incidence of adverse events (AEs) and serious adverse events (SAEs)
Zeitfenster: Up to approximately 301 days
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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.
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Up to approximately 301 days
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Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Part 1-Pharmacokinetic (PK) parameter: Cmax of DCY636
Zeitfenster: up to Day 202
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Cmax is the maximum (peak) observed blood concentration of DCY636 after dose administration.
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up to Day 202
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Part 1-Pharmacokinetic (PK) parameter: AUC of DCY636
Zeitfenster: up to Day 202
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AUC is the area under the plasma concentration-time curve.
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up to Day 202
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Part 1-Anti-drug antibodies against DCY636
Zeitfenster: up to Day 202
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To assess immunogenicity (IG) of DCY636.
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up to Day 202
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Part 2-Pharmacokinetic (PK) parameter: Cmax of DCY636
Zeitfenster: up to Day 301
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Cmax is the maximum (peak) observed blood concentration of DCY636 after dose administration.
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up to Day 301
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Part 2-Pharmacokinetic (PK) parameter: AUC of DCY636
Zeitfenster: up to Day 301
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AUC is the area under the plasma concentration-time curve.
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up to Day 301
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Part 2-Anti-drug antibodies against DCY636
Zeitfenster: up to Day 301
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To assess immunogenicity (IG) of DCY636.
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up to Day 301
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Mitarbeiter und Ermittler
Sponsor
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Primärer Abschluss (Geschätzt)
Studienabschluss (Geschätzt)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
- Genetische Krankheiten, angeboren
- Erkrankungen des Immunsystems
- Überempfindlichkeit, sofort
- Überempfindlichkeit
- Hautkrankheiten
- Hautkrankheiten, genetisch
- Hautkrankheiten, Ekzem
- Dermatitis
- Angeborene, erbliche und neonatale Krankheiten und Anomalien
- Haut- und Bindegewebserkrankungen
- Dermatitis, atopisch
- Ekzem
Andere Studien-ID-Nummern
- CDCY636A02101
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
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