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Completed Phase 3 Interventional Results available

A Study of Safety and Efficacy of MK-1986 (Tedizolid Phosphate) and Comparator in Participants From Birth to Less Than 12 Years of Age With Acute Bacterial Skin and Skin Structure Infections (MK-1986-018)

ClinicalTrials.gov ID: NCT03176134

Public ClinicalTrials.gov record NCT03176134. 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 21, 2026, 12:04 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 III Randomized, Active-comparator-Controlled Clinical Trial to Study the Safety and Efficacy of MK-1986 (Tedizolid Phosphate) and Comparator, in Subjects From Birth to Less Than 12 Years of Age With Acute Bacterial Skin and Skin Structure Infections (ABSSSI)

Brief summary

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

This study will evaluate the safety, tolerability, and efficacy of tedizolid phosphate (MK-1986) compared with comparator antibacterial agent in participants from birth to less than 12 years of age with acute bacterial skin and skin structure infections (ABSSSI).

Study identification

NCT ID
NCT03176134
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Merck Sharp & Dohme LLC
Industry
Enrollment
100 participants

Conditions and interventions

Eligibility (public fields only)

Age range
1 Day to 11 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
Jan 20, 2019 (Actual)
Primary completion
Jul 6, 2023 (Actual)
Completion
Jul 6, 2023 (Actual)
Last update posted
Jul 31, 2025

2019 – 2023

United States locations

U.S. sites
8
U.S. states
6
U.S. cities
8
Facility City State ZIP Site status
Rady Children's Hospital-San Diego ( Site 0118) San Diego California 92123 —
Ann & Robert H. Lurie Children's Hospital of Chicago ( Site 0129) Chicago Illinois 60611 —
Children's Hospital of Michigan ( Site 0100) Detroit Michigan 48201 —
William Beaumont Hospital ( Site 0108) Royal Oak Michigan 48073 —
St. Louis Children's Hospital ( Site 0127) St Louis Missouri 63110 —
Cook Children's Medical Center ( Site 0124) Fort Worth Texas 76104 —
Baylor College of Medicine - Texas Children's Hospital ( Site 0107) Houston Texas 77030 —
Children's Hospital of Richmond at VCU ( Site 0123) Richmond Virginia 23219 —

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 50 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03176134, 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 Jul 31, 2025 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03176134 live on ClinicalTrials.gov.

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