Phase 2a Study to Evaluate the Safety/Tolerability and Efficacy of TOP1288 200 mg Rectal Solution Once Daily for 4 Weeks in Ulcerative Colitis

Ulcerative Colitis Clinical Trial

— TOP2  

Official title:

A Phase 2a, Randomised, Double-Blind, Placebo-Controlled Study to Evaluate the Safety/Tolerability and Efficacy of TOP1288 200 mg Rectal Solution Once Daily for 4 Weeks in Symptomatic Ulcerative Colitis Patients With Moderate to Severe Disease Activity

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02888379
• Other study ID #: TOP1288-TV-02
• Status: Completed
• Phase: Phase 2
• First received: August 30, 2016
• Last updated: July 6, 2017
• Start date: September 2016
• Est. completion date: June 28, 2017

Study information

• Verified date: July 2017
• Source: Topivert Pharma Ltd
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

A Phase 2a, Randomised, Double-Blind, Placebo-Controlled Study to Evaluate the Safety/Tolerability and Efficacy of TOP1288 200 mg Rectal Solution Once Daily for 4 Weeks in Symptomatic Ulcerative Colitis Patients with Moderate to Severe Disease Activity

Description:

TOP1288, the first in a new class of agents called narrow spectrum protein kinase inhibitors (NSKIs), is being developed as a novel, non-absorbed treatment for ulcerative colitis (UC). UC is a disease of unknown cause characterised by inflammation of the lining of the large intestine and manifesting with abdominal pain and bloody diarrhoea. TOP1288 given rectally has a local anti-inflammatory action in experimental models of UC.

A Phase I placebo-controlled, single ascending dose (SAD) and multiple ascending dose (MAD) study of TOP1288 conducted in 61 healthy volunteers demonstrated that rectal administration of TOP1288 at doses up to 200 mg BID for 4 days was safe and well tolerated, with minimal systemic absorption. TOP1288 200 mg, administered once daily, therefore offers the potential for a safe and effective novel approach to treating patients with this serious condition.

This Phase 2a proof-of-concept study will evaluate the 200 mg daily dose of TOP1288, based on its favourable tolerability in the Phase 1 study. It will be administered as TOP1288 200 mg Rectal Solution compared against Placebo Rectal Solution, which contains all non-active excipients present in the active solution. This is a randomised, double-blind, placebo-controlled multicentre study designed to evaluate the safety/tolerability and efficacy of TOP1288 200 mg Rectal Solution following once-daily bedtime treatment for 4 consecutive weeks. The study will include approximately 40 sites in Europe. Randomization to study treatment will be 2:1, with approximately 40 subjects randomised to TOP1288 and approximately 20 subjects randomised to placebo.

The Screening period will be up to 28 days prior to the first day of dosing with double-blind study treatment (Visit 1). A central reading facility will be used to determine eligibility based upon the Screening flexible sigmoidoscopy.

Visit 2 is scheduled for Day 7 of dosing, and Visit 3 for Day 29 of dosing. There will be a 1-week safety follow-up period after Visit 3. The total duration of study participation for a given subject will be up to ~65 days or 9 weeks

Recruitment information / eligibility

• Status: Completed
• Enrollment: 77
• Est. completion date: June 28, 2017
• Est. primary completion date: June 28, 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Key Inclusion Criteria:

• Diagnosis of UC of at least 3 months duration

• Active UC with a Partial Mayo Clinic Score of 4 to 8 at randomization

Key Exclusion Criteria:

• Receiving any rectally administered medication

• Use of biologic agents within 3 months prior to Screening endoscopy

• Use of IV corticosteroids within 4 weeks prior to Screening endoscopy

• Use of oral corticosteroids at a dose >30 mg/day (or budesonide >9 mg/day).

• Patients who have started receiving immune suppressants within 3 months of the Screening endoscopy should not be included.

• Known or suspected pancolitis (unless on oral 5-ASA, steroids or permitted immunomodulators)

• Known or suspected Crohn's disease, indeterminate colitis, microscopic colitis, ischaemic colitis, or radiation-induced colitis, based on medical history, endoscopy, and/or histological findings

• Extensive (>50%) colonic resection or colectomy, or prior history of toxic megacolon within 3 months of Screening

• Patient has active serious infection (e.g., sepsis, pneumonia, abscess) or has had a serious infection (resulting in hospitalisation or requiring parenteral antibiotic treatment) within 6 weeks prior to IMP administration

• Patients testing positive of Clostridium difficile toxin or confirmed with bacterial or parasitical GI infections at Screening

Related Conditions & MeSH terms

• Colitis
• Colitis, Ulcerative
• Ulcer
• Ulcerative Colitis

Intervention

Drug:
• TOP1288

• Placebo (for TOP1288)

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Topivert Pharma Ltd

Countries where clinical trial is conducted

Bulgaria,  Czechia,  Hungary,  Latvia,  Lithuania,  Poland,  Ukraine,  United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Efficacy as measured by the Mayo Clinic modified endoscopic subscore		After 4 consecutive weeks of daily bedtime treatment
Secondary	Safety as measured by adverse events		To 1 week after the last dose
Secondary	Safety as measured by vital signs		To 1 week after the last dose
Secondary	Safety as measured by ECGs		To 1 week after the last dose
Secondary	Safety as measured by clinical laboratory tests		To 1 week after the last dose
Secondary	Efficacy as measured by Ulcerative Colitis Endoscopic Index of Severity (UCEIS) score		After 4 consecutive weeks of daily bedtime treatment
Secondary	Efficacy as measured by Partial Mayo Clinic score (i.e., the sum of the endoscopic, rectal bleeding, and stool frequency subscores)		After 4 consecutive weeks of daily bedtime treatment
Secondary	Efficacy as measured by endoscopic healing (indicated by the Mayo Clinic modified endoscopic subscore)		After 4 consecutive weeks of daily bedtime treatment
Secondary	Efficacy as measured by rectal bleeding (indicated by the Mayo Clinic rectal bleeding subscore)		After 4 consecutive weeks of daily bedtime treatment