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Completed Phase 2 Interventional

A Study of SMT19969 Compared With Vancomycin for the Treatment of Clostridium Difficile-Associated Diarrhoea (CDAD)

ClinicalTrials.gov ID: NCT02092935

Public ClinicalTrials.gov record NCT02092935. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 8:57 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase II, Randomized, Double-Blind, Active-Controlled Clinical Study to Investigate the Efficacy and Safety of SMT19969 Compared With Vancomycin for the Treatment of Clostridium Difficile-Associated Diarrhoea (CDAD)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this research study is to evaluate the safety and effectiveness of a new oral antibiotic called SMT19969 in treating C. difficile Infection (CDI).

Study identification

NCT ID
NCT02092935
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Summit Therapeutics
Industry
Enrollment
100 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 90 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 2014 (Type not available)
Primary completion
Oct 2015 (Actual)
Completion
Oct 2015 (Actual)
Last update posted
Oct 20, 2016

2014 – 2015

United States locations

U.S. sites
24
U.S. states
16
U.S. cities
24
Facility City State ZIP Site status
Not listed Mobile Alabama — —
Not listed Laguna Hills California — —
Not listed Long Beach California — —
Not listed Sylmar California — —
Not listed Ventura California — —
Not listed Idaho Falls Idaho — —
Not listed Chicago Illinois — —
Not listed Topeka Kansas — —
Not listed Baltimore Maryland — —
Not listed Boston Massachusetts — —
Not listed Detroit Michigan — —
Not listed Duluth Minnesota — —
Not listed Minneapolis Minnesota — —
Not listed Tupelo Mississippi — —
Not listed Billings Montana — —
Not listed Butte Montana — —
Not listed Sommers Point New Jersey — —
Not listed Rochester New York — —
Not listed Akron Ohio — —
Not listed Cincinnati Ohio — —
Not listed Columbus Ohio — —
Not listed Lima Ohio — —
Not listed Rapid City South Dakota — —
Not listed Seattle Washington — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02092935, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 20, 2016 · Synced Oct 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02092935 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →