Phase 2a Study of CG400549 for the Treatment of cABSSSI Caused by Methicillin-resistant Staphylococcus Aureus

CrystalGenomics

Status and phase: Completed; Phase 2

Conditions: Skin Infection

Treatments: Drug: CG400549

Study type: Interventional

Funder types: Industry

Identifiers

NCT01593761

CG400549-2-01

Details and patient eligibility

About

Primary Objective:

To make a preliminary assessment of the efficacy of CG400549 (960 mg daily) in subjects with cABSSSI (major cutaneous abscesses) due to MRSA.

Secondary Objective(s):

• To assess the pharmacokinetics of CG400549 (960 mg daily) in subjects with cABSSSI due to MRSA
• To explore the in vitro susceptibility of cABSSSI-related bacteria to CG400549.
• To assess the safety of multiple doses of CG400459

Full description

This will be an open-label, exploratory study to evaluate the safety, pharmacokinetics, and efficacy of CG400549, daily for 10 to 14 days, in subjects with cABSSSI (major cutaneous abscesses) due to MRSA. All subjects will receive active treatment.

Subjects will begin study treatment upon confirmation of clinical eligibility (ie, confirmation of MRSA infection is not required pretreatment). Subjects who begin treatment with CG400549 and are subsequently not found to have S. aureus infection will be discontinued from study treatment, treated as appropriate for the identified pathogen(s), and followed for safety. These subjects will be included in the safety analyses but not in the primary efficacy analysis.

Enrollment: 20 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Diagnosis of major cutaneous abscess suspected or confirmed to be caused by a MRSA.
2. Signs and symptoms should include at least 2 of the following: purulent drainage or discharge, erythema, fluctuance, heat or localized warmth, edema/induration, pain or tenderness to palpation

Exclusion criteria

1. Prior systemic or topical antibacterial therapy
2. Severe sepsis or refractory shock

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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20 participants in 1 patient group

Single Arm for CG400549

Experimental group

Description:

All the patients will be administered with CG400549.

Treatment:

Drug: CG400549