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Phase 2 N=85 Randomized Double-blind Treatment

Safety, Tolerability, Pharmacokinetics, and Efficacy of JBT-101 (Lenabasum) in Cystic Fibrosis

Cystic Fibrosis

Enrolled (actual)
85
Serious AEs
5.3%
Results posted
Feb 2018
Primary outcome: Primary: Number of Participants With Treatment Emergent Adverse Events. — 14; 13; 15; 21 Participants

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
JBT-101 (lenabasum) (Drug); Placebo (Other)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Corbus Pharmaceuticals Inc.
Primary completion
Dec 2016

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants With Treatment Emergent Adverse Events.
14; 13; 15; 21; 19; 14
SECONDARY
JBT-101 (Lenabasum) Plasma Concentrations on Day 84
249.77; 360.80; 0.00

Summary

The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics, and efficacy of JBT-101 in adult subjects with cystic fibrosis (CF).

Eligibility Criteria

Inclusion Criteria

  • Documentation of a CF diagnosis as evidenced by 1 or more clinical features consistent with the CF phenotype and 1 or more of the following criteria:
  • Sweat chloride equal to or greater than 60 mEq/L by quantitative pilocarpine iontophoresis test;
  • Two well-characterized mutations in the CFTR gene
  • FEV1 ≥ 40% predicted corrected
  • Stable treatment of CF for 14 days before Visit 1

Exclusion Criteria

  • Severe or unstable CF, such as:
  • Intravenous antibiotic treatment within 14 days before Visit 1
  • Treatment with any corticosteroids > 10 mg per day or > 20 mg every other day oral prednisone or equivalent within 14 days before Visit 1
  • Any one of the following values for laboratory tests at Screening:
  • A positive pregnancy test (or at Visit 1);
  • Hemoglobin 2.5 x upper normal limit
  • Total bilirubin ≥ 1.5 x upper limit of normal
  • Any other condition that, in the opinion of the Principal Investigator, is clinically significant and may put the subject at greater safety risk, influence response to study product, or interfere with study assessments.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02465450). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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