MedPath

First in Human of Single and Multiple Doses of MOR106

Phase 1
Completed
Conditions
Healthy
Dermatitis, Atopic
Interventions
Drug: Placebo single ascending doses, intravenous
Drug: MOR106 multiple ascending doses, intravenous
Drug: MOR106 single ascending doses, intravenous
Drug: Placebo multiple intravenous administrations
Registration Number
NCT02739009
Lead Sponsor
Galapagos NV
Brief Summary

This is a randomized, double-blind, placebo-controlled, dose-escalation, phase I study for the assessment of safety, tolerability and pharmacokinetics of single ascending doses of MOR106 in healthy male subjects and multiple ascending doses in subjects with moderate to severe atopic dermatitis.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
81
Inclusion Criteria
  • Able and willing to give voluntary written informed consent

Single ascending dose (SAD)

  • Negative urine drug screen
  • Male between 18-50 years of age
  • A body mass index (BMI) between 18-30 kg/m², inclusive.
  • Judged to be in good health

Multiple ascending dose (MAD)

  • Male or female between 18-65 years of age
  • A BMI between 18-30 kg/m²
  • Diagnosis of Atopic Dermatitis (AD) for at least 6 months as per the Hanifin and Rajka Criteria
  • EASI ≥ 16 at the screening and baseline visits
  • IGA score ≥3 (on the 0 to 4 IGA scale, in which 3 is moderate and 4 is severe) at the screening and baseline visits
  • Greater than or equal to 10% body surface area (BSA) of AD involvement at screening
  • Willingness to continue stable use of an additive free, basic, bland emollient twice daily for at least 7 days before the baseline visit
  • Subject is a candidate for systemic therapy and is not responding adequately or has a contraindication to topical corticosteroids and/or topical calcineurin inhibitors (per Investigator's judgement)
  • Absence of current active, latent or history of tuberculosis (TB) infection based on medical history and as determined by a negative QuantiFERON TB Gold test at screening
  • Female subjects must have a negative serum pregnancy test at screening and a negative urine pregnancy test at baseline
  • Female subjects of childbearing potential must use a highly effective method contraception from 28 days prior to the first dose of study drug, during the study and for at least 24 weeks after the last dose
Exclusion Criteria
  • Known hypersensitivity to study drug ingredients.
  • History of or a current immunosuppressive condition
  • Symptoms of clinically significant illness in the 3 months before the initial study drug administration.
  • Any concurrent illness, condition, disability, or clinically significant abnormality
  • Treatment with any drug known to have a well-defined potential for toxicity to a major organ in the last 3 months preceding the initial study drug administration.
  • A history of significant psychological, neurologic, hepatic, renal, endocrine, cardiovascular, gastrointestinal (GI), pulmonary, or metabolic disease.

MAD only

  • Active (skin) infection requiring systemic antibiotics
  • immunosuppressive/immunomodulating drugs or phototherapy 4 weeks prior to baseline
  • Treatment with topical corticosteroids (TCS) or topical calcineurin inhibitors (TCI) within 2 weeks before the baseline
  • Treatment with biologics within 5 half-lives (if known) or 12 weeks prior to baseline visit
  • history of immunosuppression
  • Regular use (more than 2 visits per week) of a tanning booth/ parlor within 4 weeks of the screening visit
  • Regular daily use of oral nonsteroidal anti-inflammatory drugs (NSAIDs), except low-dose aspirin (≤200 mg/day) for cardioprotection, within 7 days prior to screening

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
PlaceboPlacebo single ascending doses, intravenousSingle intravenous administration of Placebo
MOR106 MADMOR106 multiple ascending doses, intravenousMultiple intravenous administration of MOR106
MOR106MOR106 single ascending doses, intravenousSingle intravenous administration of MOR106
Placebo MADPlacebo multiple intravenous administrationsMultiple intravenous adminstration of Placebo
Primary Outcome Measures
NameTimeMethod
Difference as compared to placebo in the number of subjects with deviating physical examination resultsUp to 99 days after dosing

To evaluate the safety and tolerability of single ascending doses of MOR106 intravenously given to healthy male subjects and of multiple ascending doses of MOR106 given intravenously to subjects with atopic dermatitis, compared to placebo

Difference as compared to placebo in the number of subjects with abnormal vital signsUp to 99 days after dosing

To evaluate the safety and tolerability of single ascending doses of MOR106 intravenously given to healthy male subjects and of multiple ascending doses of MOR106 given intravenously to subjects with atopic dermatitis, compared to placebo

Difference as compared to placebo in the number of subjects with abnormal 12-lead ECG resultsUp to 99 days after dosing

To evaluate the safety and tolerability of single ascending doses of MOR106 intravenously given to healthy male subjects and of multiple ascending doses of MOR106 given intravenously to subjects with atopic dermatitis, compared to placebo

Difference as compared to placebo in the number of subjects with treatment-emergent adverse eventsUp to 99 days after dosing

To evaluate the safety and tolerability of single ascending doses of MOR106 intravenously given to healthy male subjects and of multiple ascending doses of MOR106 given intravenously to subjects with atopic dermatitis, compared to placebo

Difference as compared to placebo in the number of subjects with abnormal laboratory findingsUp to 99 days after dosing

To evaluate the safety and tolerability of single ascending doses of MOR106 intravenously given to healthy male subjects and of multiple ascending doses of MOR106 given intravenously to subjects with atopic dermatitis, compared to placebo

Difference as compared to placebo in the occurrence of infusion related reactionsUp to 99 days after dosing

To evaluate the safety and tolerability of single ascending doses of MOR106 intravenously given to healthy male subjects and of multiple ascending doses of MOR106 given intravenously to subjects with atopic dermatitis, compared to placebo

Secondary Outcome Measures
NameTimeMethod
Serum concentration (Cinf) of MOR106up to 99 days after dosing

To characterize the PK of MOR106 after single intravenous administration in healthy male volunteers and after multiple ascending dose intravenous administration in subjects with severe atopic dermatitis

Area under the curve (AUC) of MOR106up to 99 days after dosing

To characterize the PK of MOR106 after single intravenous administration in healthy male volunteers and after multiple ascending dose intravenous administration in subjects with severe atopic dermatitis

terminal elimination half-life (t1/2) of MOR106up to 99 days after dosing

To characterize the PK of MOR106 after single intravenous administration in healthy male volunteers and after multiple ascending dose intravenous administration in subjects with severe atopic dermatitis

total serum clearance (CL) of MOR106up to 99 days after dosing

To characterize the PK of MOR106 after single intravenous administration in healthy male volunteers and after multiple ascending dose intravenous administration in subjects with severe atopic dermatitis

volume of distribution at steady state (Vss) of MOR106up to 99 days after dosing

To characterize the PK of MOR106 after single intravenous administration in healthy male volunteers and after multiple ascending dose intravenous administration in subjects with severe atopic dermatitis

The presence of anti-drug antibodies in serum over time after single intravenous doseup to 9 days after dosing

To assess the presence of anti-drug antibodies as a measure of immunogenicity after single administration of MOR106 and after multiple ascending dose intravenous administration in subjects with severe atopic dermatitis

Trial Locations

Locations (4)

• Arensia Phase I unit

🇲🇩

Chisinau, Moldova, Republic of

SGS LSS Clinical Pharmacology Unit

🇧🇪

Antwerp, Belgium

Arensia Phase I unit

🇷🇴

Bucharest, Romania

St Johns Hospital

🇭🇺

Budapest, Hungary

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