Defined Bacterial Consortia

Defined bacterial consortia as a differentiated modality to target gastrointestinal (GI) diseases (H2 relative to H1)

We are developing defined bacterial consortia as oral therapies to treat a wide range of debilitating diseases across multiple therapeutic areas, with an initial focus on gastrointestinal (GI) diseases in which gut dysbiosis — a disruption of the gut microbiota— is a known disease driver.

Gut Microbiota and its Role in Human Health (H3)

We are developing defined bacterial consortia as oral therapies to treat a wide range of debilitating diseases across multiple therapeutic areas, with an initial focus on gastrointestinal (GI) diseases in which gut dysbiosis — a disruption of the gut microbiota— is a known disease driver.

Clinical Research Study
for Ulcerative Colitis

Phase 3 Study for
Prevention of Recurrent CDI

RESTORATiVE303 is a double-blind, placebo-controlled, Phase 3 study to evaluate the safety and efficacy of a 14-day course of VE303. The efficacy of VE303 will be assessed by comparing the Clostridioides difficile infection (CDI) recurrence rate at Week 8 in study participants who receive VE303 and those who receive placebo.

A Live Biotherapeutic Product (LBP) is a biological product that: 
1) contains live organisms, such as bacteria; 2) is applicable to the prevention, treatment, or cure of a disease or condition of human beings; and 3) is not a vaccine.

Cilinical Trials

Clinical Research Study
for Ulcerative Colitis

Phase 3 Study for
Prevention of Recurrent CDI

Clinical Trial

We are currently conducting COLLECTiVE202, a randomized, double-blind, placebo-controlled, multinational Phase 2 study of VE202 in individuals with mild-to-moderate UC. The FDA has granted VE202 Fast Track designation for the treatment of adults with UC.

Manufacturing

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Intellectual Property

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Pipeline

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Pipeline

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