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
Studieoversigt
Status
Status
Betingelser
Betingelser
Intervention / Behandling
Intervention / Behandling
Detaljeret beskrivelse
Undersøgelsestype
Undersøgelsestype
Tilmelding (Anslået)
Tilmelding
Fase
Fase
- Fase 1
Kontakter og lokationer
Studiekontakt
Studiekontakt
- Navn: Novartis Pharmaceuticals
Undersøgelse Kontakt Backup
- Navn: Novartis Pharmaceuticals
- Telefonnummer: +81337978748
- E-mail: novartis.email@novartis.com
Studiesteder
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Fukuoka, Japan, 812-0025
- Rekruttering
- Novartis Investigative Site
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Deltagelseskriterier
Berettigelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
Tager imod sunde frivillige
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
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Dobbelt
Antal våben
Våben og indgreb
Deltagergruppe / ArmDeltagergruppe / Arm |
Intervention / BehandlingIntervention / Behandling |
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Eksperimentel: 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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Eksperimentel: 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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Eksperimentel: 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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Eksperimentel: 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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Eksperimentel: 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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Eksperimentel: 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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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.
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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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Deltagerne vil modtage Placebo
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Placebo komparator: Part 1- Cohort A2: Placebo
Cohort A2: Placebo in healthy participants.
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Deltagerne vil modtage Placebo
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Placebo komparator: Part 1- Cohort A3: Placebo
Cohort A3: Placebo in healthy participants.
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Deltagerne vil modtage Placebo
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Placebo komparator: Part 1- Cohort A4: Placebo
Cohort A4: Placebo in healthy participants.
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Deltagerne vil modtage Placebo
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Placebo komparator: Part 1- Cohort B1: Placebo
Cohort B1: Placebo in healthy participants.
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Deltagerne vil modtage Placebo
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Placebo komparator: Part 1- Cohort B2: Placebo
Cohort B2: Placebo in healthy participants.
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Deltagerne vil modtage 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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Deltagerne vil modtage Placebo
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Hvad måler undersøgelsen?
Primære resultatmål
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
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Part 1-Incidence of adverse events (AEs) and serious adverse events (SAEs)
Tidsramme: 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)
Tidsramme: 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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Sekundære resultatmål
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
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Part 1-Pharmacokinetic (PK) parameter: Cmax of DCY636
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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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Samarbejdspartnere og efterforskere
Sponsor
Sponsor
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Studiestart
Primær færdiggørelse (Anslået)
Primær færdiggørelse
Studieafslutning (Anslået)
Studieafslutning
Datoer for studieregistrering
Først indsendt
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Først opslået
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering sendt
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
Andre undersøgelses-id-numre
- CDCY636A02101
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
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