Vedanta Biosciences

Vedanta Biosciences

Develops microbiome-based therapies using bacteria

About Vedanta Biosciences

Simplify's Rating
Why Vedanta Biosciences is rated
A
Rated A on Competitive Edge
Rated B on Growth Potential
Rated A+ on Rating Differentiation

Industries

Biotechnology

Healthcare

Company Size

51-200

Company Stage

Late Stage VC

Total Funding

$364.5M

Headquarters

Cambridge, Massachusetts

Founded

2010

Overview

Vedanta Biosciences focuses on developing microbiome therapies using groups of beneficial bacteria known as bacterial consortia. These consortia can colonize the human intestine and have the potential to treat various diseases. The company utilizes a proprietary discovery platform to identify and assemble these bacteria into effective therapeutic teams. Unlike many competitors, Vedanta has achieved commercial-scale production of its drug candidates while adhering to strict FDA regulations for safety and quality. The goal of Vedanta Biosciences is to transform healthcare by providing new treatment options through its innovative approach to drug discovery.

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Simplify's Take

What believers are saying

  • Fast Track designation for VE303 accelerates regulatory approval process.
  • Phase 3 RESTORATiVE303 study positions Vedanta as a market leader for rCDI.
  • Recent $106.5M funding round strengthens financial position and growth potential.

What critics are saying

  • Competition from Seres Therapeutics with FDA-approved C. difficile treatment.
  • High production costs may impact profitability and market reach.
  • Regulatory challenges due to unclear FDA guidelines for microbiome therapies.

What makes Vedanta Biosciences unique

  • Vedanta uses defined bacterial consortia for consistent therapeutic outcomes.
  • First to achieve commercial-scale CGMP production of bacterial consortia drugs.
  • Proprietary platform identifies and assembles optimal bacterial consortia for therapies.

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Funding

Total Funding

$364.5M

Above

Industry Average

Funded Over

4 Rounds

Late VC funding comparison data is currently unavailable. We're working to provide this information soon!
Late VC Funding Comparison
Coming Soon

Growth & Insights and Company News

Headcount

6 month growth

-2%

1 year growth

0%

2 year growth

2%
PharmiWeb
May 22nd, 2024
Vedanta Biosciences Enrolls First Patient In Pivotal Phase 3 Restorative303 Study Of Ve303 For The Prevention Of Recurrent C. Difficile Infection

VE303 is an orally administered, potential first-in-class live biotherapeutic product candidate being developed to prevent recurrence of Clostridioides difficile infection (CDI). CAMBRIDGE, MA, May 21, 2024 – Vedanta Biosciences, a clinical-stage company that is developing a potential new category of oral therapies based on defined bacterial consortia, today announced that the first patient has been dosed in the global Phase 3 RESTORATiVE303 clinical study. VE303 is an orally administered defined bacterial consortium candidate that is being developed for the prevention of recurrent C. difficile infection (rCDI). The RESTORATiVE303 trial is evaluating the efficacy and safety of VE303 in patients with rCDI and is intended to form the basis for a Biologics License Application (BLA) to be filed with the U.S. Food and Drug Administration

Business Wire
May 21st, 2024
Puretech Founded Entity Vedanta Biosciences Enrolls First Patient In Pivotal Phase 3 Restorative303 Study Of Ve303 For The Prevention Of Recurrent C. Difficile Infection

BOSTON--(BUSINESS WIRE)--PureTech Health plc (Nasdaq: PRTC, LSE: PRTC) ("PureTech" or the "Company"), a clinical-stage biotherapeutics company, noted today that its Founded Entity, Vedanta Biosciences, a clinical-stage company that is developing a potential new category of oral therapies based on defined bacterial consortia, announced that the first patient has been dosed in the global Phase 3 RESTORATiVE303 clinical study of VE303, which is an orally administered defined bacterial consortium candidate that is being developed for the prevention of recurrent C. difficile infection (rCDI). The RESTORATiVE303 trial is evaluating the efficacy and safety of VE303 in patients with rCDI and is intended to form the basis for a Biologics License Application to be filed with the U.S. Food and Drug Administration. The full text of the announcement from Vedanta is as follows:. Vedanta Biosciences Enrolls First Patient in Pivotal Phase 3 RESTORATiVE303 Study of VE303 for the Prevention of Recurrent C

Business Wire
May 21st, 2024
Vedanta Biosciences Enrolls First Patient In Pivotal Phase 3 Restorative303 Study Of Ve303 For The Prevention Of Recurrent C. Difficile Infection

CAMBRIDGE, Mass.--(BUSINESS WIRE)--Vedanta Biosciences, a clinical-stage company that is developing a potential new category of oral therapies based on defined bacterial consortia, today announced that the first patient has been dosed in the global Phase 3 RESTORATiVE303 clinical study. VE303 is an orally administered defined bacterial consortium candidate that is being developed for the prevention of recurrent C. difficile infection (rCDI). The RESTORATiVE303 trial is evaluating the efficacy and safety of VE303 in patients with rCDI and is intended to form the basis for a Biologics License Application (BLA) to be filed with the U.S. Food and Drug Administration. “Initiation of the RESTORATiVE303 study represents a key clinical milestone for the VE303 program

Business News This Week
Feb 23rd, 2024
Colorcon Ventures Invests in Vedanta Biosciences, a Clinical-Stage Microbial Therapeutics Company

Colorcon Ventures joins a prominent list of investors who also participated in Vedanta’s fundraising round, including AXA IM Alts, The AMR Ac

LiveMint
Oct 17th, 2023
Vedanta exploring tie-ups with Japanese tech firms for semiconductor plants

Premium Earlier, Vedanta had formed a joint venture with Taiwanese electronics manufacturing giant Foxconn which announced plans to invest $19.5 billion in setting up a semiconductor wafer fabrication plant.

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