Not provided
| ID | Type | Description | Link |
|---|---|---|---|
| HHSO100201700014C | Other Identifier | Department of Health and Human Services |
Not provided
Not provided
SMT19969-C006 study was terminated in alignment with corporate decision to pursue further development of drug candidate with a partner.
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| Name | Class |
|---|---|
| Department of Health and Human Services | FED |
Not provided
Not provided
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Not provided
Study to evaluate the safety of ridinilazole in adolescent subjects and how ridinilazole is metabolized.
Not provided
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Ridinilazole | Experimental | Ridinilazole dosed BID and a comparator placebo dosed QID, to maintain blind, for 40 doses over 10 days. |
|
| Vancomycin | Active Comparator | Vancomycin dosed QID and a Ridinilazole placebo dosed BID, to maintain blind, for 40 doses over 10 days. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Ridinilazole | Drug | Ridinilazole 200mg dosed BID for 10 days. |
| |
| Measure | Description | Time Frame |
|---|---|---|
| Incidence and Severity of Treatment-emergant Adverse Events | Safety was assessed using CTCAE v4. | Until study completion (Day 100) |
Not provided
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
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Not provided
| Name | Affiliation | Role |
|---|---|---|
| Lori Styles, MD | Summit Therapeutics | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of California, Los Angeles (UCLA) David Geffen School of Medicine | Los Angeles | California | 90095 | United States | ||
Not provided
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| ID | Title | Description |
|---|---|---|
| FG000 | Ridinilazole | Ridinilazole dosed BID and a comparator placebo dosed QID, to maintain blind, for 40 doses over 10 days. Ridinilazole: Ridinilazole 200mg dosed BID for 10 days. |
| FG001 | Vancomycin |
| Title | Milestones | Reasons Not Completed | |||||
|---|---|---|---|---|---|---|---|
| Overall Study |
|
Not provided
Not provided
| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot | Yes | No | No | Study Protocol | Nov 12, 2021 | Jan 25, 2023 |
Not provided
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| Vancomycin |
| Drug |
Vancomycin 125mg dosed QID for 10 days. |
|
| Children's Hospital Orange County |
| Orange |
| California |
| 92868 |
| United States |
| Continental Clinical Research | Miami | Florida | 33144 | United States |
| Dynamic Medical Research LLC | Miami | Florida | 33144 | United States |
| D&H National Research Centers | Miami | Florida | 33155 | United States |
| HMD Research | Orlando | Florida | 32819 | United States |
| Children's Center for Digestive Health | Atlanta | Georgia | 30342 | United States |
| Snake River Research | Idaho Falls | Idaho | 83404 | United States |
| Ann and Robert H Lurie Children's Hospital of Chicago | Chicago | Illinois | 60611 | United States |
| University of Chicago - Comer Children's Hospital | Chicago | Illinois | 60637 | United States |
| Indiana University Health - Riley Hospital for Children | Indianapolis | Indiana | 46202 | United States |
| Boston Children's Hospital | Boston | Massachusetts | 02115 | United States |
| Children's Hospital of Michigan | Detroit | Michigan | 48201 | United States |
| Icahn School of Medicine at Mount Sinai | New York | New York | 10029 | United States |
| DiGiovanna Institute for Medical Education and Research | New York | New York | 11758 | United States |
| Stony Brook University Medical Center | Stony Brook | New York | 11794 | United States |
| Cincinnati Children's Hospital Medical Center | Cincinnati | Ohio | 45229 | United States |
| University Hospitals Cleveland Medical Center - Rainbow Babies and Children's Hospital | Cleveland | Ohio | 44106 | United States |
Vancomycin dosed QID and a Ridinilazole placebo dosed BID, to maintain blind, for 40 doses over 10 days.
Vancomycin: Vancomycin 125mg dosed QID for 10 days.
| COMPLETED |
|
| NOT COMPLETED |
|
Not provided
| ID | Title | Description |
|---|---|---|
| BG000 | Ridinilazole | Ridinilazole dosed BID and a comparator placebo dosed QID, to maintain blind, for 40 doses over 10 days. Ridinilazole: Ridinilazole 200mg dosed BID for 10 days. |
| BG001 | Vancomycin | Vancomycin dosed QID and a Ridinilazole placebo dosed BID, to maintain blind, for 40 doses over 10 days. Vancomycin: Vancomycin 125mg dosed QID for 10 days. |
| BG002 | Total | Total of all reporting groups |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Age, Categorical | Count of Participants | Participants |
| ||||||||||||||||||
| Sex: Female, Male | Count of Participants | Participants |
| ||||||||||||||||||
| Ethnicity (NIH/OMB) | Count of Participants | Participants |
| ||||||||||||||||||
| Race (NIH/OMB) | Count of Participants | Participants |
|
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | |||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Incidence and Severity of Treatment-emergant Adverse Events | Safety was assessed using CTCAE v4. | No analysis was done for study outcome measures due to the fact that enrollment in the clinical trial did not reach the target number of subjects needed prior to study termination and was insufficient to produce statistically reliable results. | Posted | Count of Participants | Participants | Until study completion (Day 100) |
|
|
|
Until study completion (Day 100)
No adverse event was reported throughout the duration of the study.
Not provided
| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Ridinilazole | Ridinilazole dosed BID and a comparator placebo dosed QID, to maintain blind, for 40 doses over 10 days. Ridinilazole: Ridinilazole 200mg dosed BID for 10 days. | 0 | 1 | 0 | 1 | 0 | 1 |
| EG001 | Vancomycin | Vancomycin dosed QID and a Ridinilazole placebo dosed BID, to maintain blind, for 40 doses over 10 days. Vancomycin: Vancomycin 125mg dosed QID for 10 days. | 0 | 1 | 0 | 1 | 0 | 1 |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Katie Tran | Summit Therapeutics | 4086776503 | Katie.Tran@Summitplc.com |
| Prot_000.pdf |
Not provided
| ID | Term |
|---|---|
| D003015 | Clostridium Infections |
| D003967 | Diarrhea |
| D007239 | Infections |
| ID | Term |
|---|---|
| D016908 | Gram-Positive Bacterial Infections |
| D001424 | Bacterial Infections |
| D001423 | Bacterial Infections and Mycoses |
| D012817 | Signs and Symptoms, Digestive |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |
Not provided
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| ID | Term |
|---|---|
| C000601750 | ridinilazole |
| D014640 | Vancomycin |
| ID | Term |
|---|---|
| D006020 | Glycopeptides |
| D006001 | Glycoconjugates |
| D002241 | Carbohydrates |
| D010455 | Peptides |
| D000602 | Amino Acids, Peptides, and Proteins |
Not provided
Not provided
| >=65 years |
|
| Male |
|
| Not Hispanic or Latino |
|
| Unknown or Not Reported |
|
| Asian |
|
| Native Hawaiian or Other Pacific Islander |
|
| Black or African American |
|
| White |
|
| More than one race |
|
| Unknown or Not Reported |
|