SER-301 is a Biologic owned by Seres Therapeutics, and is involved in 1 clinical trial, which was completed.

SER-301 works by modulating microbe-microbe and microbe-host interactions. It alters the composition and activities of the microbial communities in the body to regulate host pathways.

The revenue for SER-301 is expected to reach a total of $1.5bn through 2038. This change impacts the valuation of this asset and is an important factor to understand the current value of the drug in a clinical process. View the complete picture with the SER-301 NPV Report.

SER-301 is originated and owned by Seres Therapeutics.

SER-301 Overview

SER-301 is under development for the treatment of ulcerative colitis. The therapeutic candidate is administered orally. It is a consortia of bacteria synthetically fermented ecobiotic, developed based on Human Microbiome Therapeutics technology. It was under development for Crohn’s disease.

Seres Therapeutics Overview

Seres Therapeutics (Seres) is a microbiome therapeutics platform company that develops a novel class of biological drugs. The company creates a new class of medicines to treat diseases resulting from functional deficiencies in the microbiome, a condition known as dysbiosis. The company’s lead development candidate, SER-109 is an oral microbiome therapeutic and bacterial spore ecology. Seres’ SER-287 is an oral therapy for the treatment of ulcerative colitis, an inflammatory bowel disease. Its development programs also include SER-301 and SER-155, which are investigational, oral, rationally designed, fermented microbiome therapeutic. The company utilizes its microbiome therapeutics platform to identify key alterations in the microbiome that are associated with or lead to specific diseases. Seres is headquartered in Cambridge, Massachusetts, the US

The company reported revenues of (US Dollars) US$144.9 million for the fiscal year ended December 2021 (FY2021), compared to a revenue of US$33.2 million in FY2020. The operating loss of the company was US$64.5 million in FY2021, compared to an operating loss of US$88.1 million in FY2020. The net loss of the company was US$65.6 million in FY2021, compared to a net loss of US$89.1 million in FY2020. The company reported revenues of US$3.4 million for the third quarter ended September 2022, compared to a revenue of US$1.2 million the previous quarter.

Quick View – SER-301

Report Segments
  • Innovator
Drug Name
  • SER-301
Administration Pathway
  • Oral
Therapeutic Areas
  • Gastrointestinal
Key Companies
Highest Development Stage
  • Phase I

GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article.

To create this model, GlobalData takes into account factors including patent law, known and projected regulatory approval processes, cash flows, potential applicable patients, drug margins, company expenses, and pricing estimates. Combining these data points with GlobalData’s world class analysis creates high value models that companies can use to help in evaluation processes for each drug or company.

The rNPV method integrates the probability of a drug reaching a clinical stage into the cash flow at that time, which provides a more accurate rNPV, as it considers the probability that the drug never makes it through the clinical pathway to commercialization. GlobalData’s rNPV model uses proprietary likelihood of approval (LoA)and phase transition success rate(PTSR) data for the indication in the highest development stage, which can be found on GlobalData’s Pharmaceutical Intelligence Center.