Etrasimod is a Small Molecule owned by Pfizer, and is involved in 26 clinical trials, of which 17 were completed, 8 are ongoing, and 1 is planned.

Etrasimod (APD-334) acts as S1P1, S1P4 and S1P5 receptor agonist. Sphingosine 1-phosphate (S1P) is an important regulator of many different immune functions including lymphocyte circulation, antigen presentation, and T cell development. S1P receptors couple to different heterotrimeric G proteins and elicit cellular signaling events by activating the small GTPases Rac and Rho and protein kinases Akt, ERK, and JNK and by inducing cellular calcium flux and inhibiting cAMP accumulation. The drug candidate by agonizing S1P receptors alleviates the disease condition.

The revenue for Etrasimod is expected to reach a total of $1.3bn 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 Etrasimod NPV Report.

Etrasimod was originated by Arena Pharmaceuticals and is currently owned by Pfizer. Everest Medicines is the other company associated in development or marketing of Etrasimod.

Etrasimod Overview

Etrasimod (APD-334) is under development for the treatment of moderately to severely active ulcerative colitis, Crohn's disease, atopic dermatitis, alopecia areta and Eosinophilic Esophagitis (EOE). The drug candidate is a next-generation small molecule and is administered through oral route. It acts by targeting S1P1, S1P4 and S1P5 receptors. It is developed based on GPCR-based drug discovery technology platform. It was also under development for autoimmune diseases such as multiple sclerosis, psoriasis, rheumatoid arthritis and dermatological extraintestinal manifestations (EIM) in patients with inflammatory bowel disease. It was also under development for pyoderma gangrenosum and primary biliary cirrhosis (cholangitis).

Everest Medicines Overview

Everest Medicines, is a biopharmaceutical company that licenses, develops and commercializes medicines for the treatment of cancer, autoimmune, cardio renal and infectious diseases. It is investigating Sacituzumab govitecan, an antibody-drug conjugate targeting metastatic triple-negative breast cancer (mTNBC), metastatic urothelial cancer (mUc), non-small cell lung cancer (NSCLC) and other oncology indications; and FGF401 for hepatocellular carcinoma. The company is evaluating Etrasimod to treat ulcerative colitis and other autoimmune diseases; Nefecon for IgA nephropathy; Ralinepag against pulmonary arterial hypertension (PAH). Everest Medicines is also developing drugs for community-acquired bacterial pneumonia (CABP), complicated urinary tract infection (cUTi) and other infectious diseases. It works in partnership with Immunomedics, Novartis, Arena Pharmaceuticals and other companies to develop its products. Everest Medicines is headquartered in Shanghai, China.

The company reported revenues of (Renminbi) CNY0.1 million for the fiscal year ended December 2021 (FY2021). The operating loss of the company was CNY1,026.3 million in FY2021, compared to an operating loss of CNY688.5 million in FY2020. The net loss of the company was CNY1,008.7 million in FY2021, compared to a net loss of CNY5,658.2 million in FY2020.

Quick View – Etrasimod

Report Segments
  • Innovator
Drug Name
  • Etrasimod
Administration Pathway
  • Oral
Therapeutic Areas
  • Central Nervous System
  • Dermatology
  • Gastrointestinal
  • Immunology
Key Companies
Highest Development Stage
  • Pre-Registration

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.