Qpex laboratory building in San Diego, California.

R&D Pipeline

We are advancing a portfolio of clinical-stage programs to comprehensively address patient needs in inpatient and outpatient settings by treating a range of multidrug-resistant pathogens. Our team has worked together for over 25 years, completing four regulatory approvals in the past decade.

We continue to make progress, having advanced three products to U.S. Investigational New Drug (IND) application stage during the companyโ€™s first three years of operations. We are combining our deep expertise with Shionogiโ€™s decades of successful infectious disease R&D in Japan to address the unmet medical needs of patients and healthcare professionals and to protect society from serious current and emerging Gram-negative bacterial infections.

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Qpex Biopharma Product Pipeline

These compounds and their uses are investigational and have not all been approved by the U.S. Food and Drug Administration. This information is presented only for purposes of providing a general overview and should not be construed as a recommendation for use of any product for unapproved uses.
Discovery
IND-Enabling
Phase 1
Phase 2
Phase 3
Focus Area: Infections Due to Gram-Negative Bacteria
Delivery Method: Intravenous Infusion
Status: Phase 1

Focus Area: Complicated Urinary Tract Infections
Delivery Method: Oral
Status: Phase 1

Other Programs

Focus Area: Resistant Bacterial Infections
Delivery Method: Intravenous Infusion and
Oral
Status: Discovery

A Shionogi Group Company