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Clinical Trials/NCT02818686
NCT02818686
Completed
Phase 1

A Phase 1b Multi-Center, Randomized, Double-Blind, Multi-Dose, Placebo-Controlled Study to Evaluate the Safety, Tolerability, Pharmacodynamics, and Plasma Exposure of TD-1473 in Subjects With Moderately-to-Severely Active Ulcerative Colitis

Theravance Biopharma1 site in 1 country40 target enrollmentOctober 3, 2016

Overview

Phase
Phase 1
Intervention
TD-1473
Conditions
Ulcerative Colitis, Active Moderate
Sponsor
Theravance Biopharma
Enrollment
40
Locations
1
Primary Endpoint
Ctrough in plasma
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

This study is designed to evaluate the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of TD-1473 in subjects with moderately-to-severely active UC over 28 days. This exploratory study will also serve as a signal seeking endeavor to demonstrate biologic effect associated with TD-1473 through biomarker analysis and clinical, endoscopic, and histologic assessments.

Registry
clinicaltrials.gov
Start Date
October 3, 2016
End Date
March 29, 2018
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Has a history of ulcerative colitis diagnosis at least 3 months prior to screening
  • Is intolerant, refractory, or only partially responsive to aminosalicylates, corticosteroids, immunomodulators, or biologics. If subject is currently receiving an oral aminosalicylate, he or she is eligible and can stay on that dose of aminosalicylate provided the dose has been stable for at least 2 weeks prior to screening. If the subject is currently receiving an oral corticosteroid, he or she is eligible if the dose is equivalent to or less than prednisone 20 mg/day or budesonide 9 mg/day and stable for at least 2 weeks prior to screening sigmoidoscopy if the subject has been on corticosteroids for more than 2 weeks.
  • Has a rectal bleeding score ≥ 1 and a bowel frequency score ≥ 1 on the patient-reported outcome 2 (PRO2) on screening sigmoidoscopy day and on Day 1 in addition to a modified Mayo endoscopic subscore of ≥ 2 during screening
  • Women of childbearing potential must have a negative pregnancy test and either abstain from sexual intercourse or use a highly effective method of birth control
  • Willing and able to give informed consent
  • Additional inclusion criteria apply

Exclusion Criteria

  • Has fulminant colitis, toxic megacolon, primary sclerosing cholangitis, Crohn's disease, history of colitis-associated colonic dysplasia, active peptic ulcer disease
  • Medications of exclusion: a) azathioprine, 6-mercaptopurine, or methotrexate within the 28 days prior to Day 1, b) adalimumab, infliximab, golimumab, etanercept, or certolizumab within the 60 days prior to Day 1, c) intravenous corticosteroids within the 14 days prior to Day 1, d) topical mesalamine or steroid (i.e., enemas or suppositories) within the 14 days prior to Day 1, e) any prior exposure to mycophenolic acid, tacrolimus, sirolimus, cyclosporine, natalizumab, rituximab, efalizumab, ustekinumab, fingolimod, or thalidomide, f) NSAIDs on a daily basis, g) tofacitinib within the 60 days prior to Day 1; h) vedolizumab within 120 days prior to Day 1
  • Has a current bacterial, parasitic, fungal, or viral infection
  • Is positive for hepatitis A, B or C, HIV or tuberculosis
  • Has clinically significant abnormalities in laboratory evaluations
  • Participated in another clinical trial of an investigational drug (or medical device) within 30 days prior to screening (or within 60 days prior to screening if investigational drug was a biologic or another Janus kinase (JAK) inhibitor, or is currently participating in another trial of an investigational drug (or medical device)
  • Use of prescription medications started or with a dose adjustment within 4 weeks prior to study enrollment, or over-the-counter medications or supplements started or with a dose adjustment within 2 weeks prior study enrollment. Anti-diarrheal medications are allowed only if dose has been stable at least 2 weeks prior to study enrollment
  • Additional exclusion criteria apply

Arms & Interventions

TD-1473 low dose

10 subjects will be randomized to receive low-dose TD-1473 orally daily for 28 days

Intervention: TD-1473

TD-1473 mid dose

10 subjects will be randomized to receive mid-dose TD-1473 orally daily for 28 days

Intervention: TD-1473

TD-1473 high dose

10 subjects will be randomized to receive high-dose TD-1473 orally daily for 28 days

Intervention: TD-1473

Placebo

10 subjects will be randomized to receive placebo orally daily for 28 days

Intervention: Placebo

Outcomes

Primary Outcomes

Ctrough in plasma

Time Frame: Day 14 (Pre-dose)

Trough Concentration of TD-1473

Electrocardiogram

Time Frame: Baseline to Day 14

Number of participants who experienced a Clinically Significant Electrocardiogram (ECG) Result

Cmax in plasma

Time Frame: Day 1 and Day 14

Maximum Observed Plasma Concentration of TD-1473

Tmax in plasma

Time Frame: Day 1 and Day 14

Time to Reach Maximum Observed Plasma Concentration (Cmax) of TD-1473

Tlast in plasma

Time Frame: Day 1 and Day 14

Time to Last Quantifiable Concentration of TD-1473

AUC0-4 in plasma

Time Frame: Day 1 and Day 14

Area Under the Concentration-time Curve from Time Zero to 4 hours Post-Dose of TD-1473

Ctissue in plasma

Time Frame: Day 28

Tissue Concentration of TD-1473

Treatment-emergent Adverse Events (TEAE)

Time Frame: Baseline to end of follow-up (a maximum of 42 days)

Number of participants who experience one or more treatment-emergent Adverse Events (TEAE)

Moderate or Severe Treatment-emergent Adverse Events (TEAE)

Time Frame: Baseline to end of follow-up (a maximum of 42 days)

Number of participants who experience one or more moderate or severe treatment-emergent Adverse Events (TEAE)

Serious Treatment-emergent Adverse Events (TEAE)

Time Frame: Baseline to end of follow-up (a maximum of 42 days)

Number of participants who experience one or more serious treatment-emergent Adverse Events (TEAE)

Clinical Laboratory Measurements

Time Frame: Baseline to end of follow-up (a maximum of 42 days)

Number of participants who experienced a Clinically Significant Clinical Laboratory Measurements

Vital Signs

Time Frame: Baseline to end of follow-up (a maximum of 42 days)

Number of participants who experienced a Clinically Significant Vital Sign Measurement

Secondary Outcomes

  • C-reactive protein (CRP)(Baseline, Day 14 and Day 28)
  • Fecal Calprotectin(Baseline and Day 28)
  • Partial Mayo score(Baseline, Day 14 and Day 28)

Study Sites (1)

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