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Everest Medicines Announces that Licensing Partner Pfizer Reports Positive Topline Results from Yearlong Phase 3 Trial of Etrasimod in Ulcerative Colitis Patients, Underscoring Best-in-Class Potential

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Everest Medicines announced that its licensing partner, Pfizer (NYSE: PFE), has reported positive topline results from the ELEVATE UC 52 Phase 3 study of etrasimod, a novel treatment for moderately to severely active ulcerative colitis (UC). In this 52-week trial, 433 patients showed significant improvements in clinical remission at both 12 and 52 weeks compared to placebo. Etrasimod demonstrated a favorable safety profile. Pfizer plans to file for regulatory approval later this year, supported by these positive trial results.

Positive
  • Etrasimod achieved statistically significant clinical remission at weeks 12 and 52 in the ELEVATE UC 52 trial.
  • All key secondary endpoints also showed statistically significant improvements.
  • Pfizer plans to initiate regulatory filings for etrasimod later this year.
Negative
  • None.

SHANGHAI, March 29, 2022 /PRNewswire/ -- Everest Medicines (HKEX 1952.HK) announced today that its licensing partner, Pfizer Inc. (NYSE: PFE) reported positive topline results from a second Phase 3 study of etrasimod, an investigational, oral, once-a-day, selective sphingosine 1-phosphate (S1P) receptor modulator in development for the treatment of moderately to severely active ulcerative colitis (UC).

In this 52-week study, also known as ELEVATE UC 52, etrasimod patients achieved statistically significant improvements in the co-primary endpoints of clinical remission at weeks 12 and 52 when compared to placebo. Statistically significant improvements were attained in all key secondary endpoints at both 12 and 52 weeks. Etrasimod demonstrated a safety profile consistent with previous studies, including the Phase 2 OASIS trial.

The global Phase 3 multi-center, randomized, double-blind, placebo-controlled study enrolled 433 UC patients who had previously failed or were intolerant to at least one conventional, biologic, or Janus kinase (JAK) inhibitor therapy. Participants received etrasimod 2 mg or placebo once-daily. ELEVATE UC 52 utilized a treat-through design in which patients were eligible to continue with their randomized treatment independent of whether they reached the objective criteria of clinical response at week 12.

Full results from the studies will be submitted for future scientific publication and presentation. The positive 12- and 52-week results from ELEVATE UC 52 follow the recent announcement of positive 12-week findings from the ELEVATE UC 12 trial earlier this month.  These data, along with results from ELEVATE UC 12 and the long-term extension from these two trials (ELEVATE UC OLE), are expected to form the basis for planned future regulatory filings. Pfizer expects to initiate regulatory filings later this year.

Etrasimod was developed by Arena Pharmaceuticals, which was recently acquired by Pfizer, and Everest Medicines secured exclusive rights from Arena to develop, manufacture and commercialize etrasimod in Greater China and South Korea in 2017. Everest Medicines is conducting a phase 3 study for etrasimod in Asia for the treatment of moderate-severe ulcerative colitis, which is expected to complete enrollment in 2023.

"We are excited to see continuing positive topline results on Etrasimod, underlying its potential as a best-in-class therapy," said Kerry Blanchard, MD, PhD, CEO of Everest Medicines. "We'll actively move forward our phase 3 study in Asia in order to bring the product to moderate-severe ulcerative colitis patients in this region as early as possible."

About Etrasimod

Etrasimod is an oral, once-a-day, selective sphingosine 1-phosphate (S1P) receptor modulator being investigated for a range of immuno-inflammatory diseases including ulcerative colitis, Crohn's Disease, atopic dermatitis, eosinophilic esophagitis, and alopecia areata.

In a Phase 2, randomized, placebo-controlled, dose-ranging study (OASIS) in moderate to severe UC patients, most patients who achieved clinical response, clinical remission, or endoscopic improvement at week 12 experienced sustained or improved effects up to week 46, with etrasimod 2 mg in the open-label extension. Etrasimod also demonstrated a favorable benefit/risk profile, consistent with safety findings reported in the double-blind portion of OASIS.

About ELEVATE UC 52

ELEVATE UC 52 is one of two pivotal trials that are part of the ELEVATE UC global Phase 3 registrational program. ELEVATE UC 52 is a 2:1 randomized, double-blind, placebo-controlled trial to assess the efficacy and safety of etrasimod 2 mg once-daily in participants with moderately-to-severely active UC. This is a one-year trial evaluating clinical remission at 12 weeks, or induction, and at 52 weeks. ELEVATE UC 52 utilized a treat-through design in which patients were eligible to continue with etrasimod independent of whether they reached clinical response at week 12.

The primary objective of this trial is to assess the safety and efficacy of etrasimod on clinical remission after both 12 and 52 weeks. The primary endpoint is based on the 3-domain, modified Mayo score. Key secondary measures include the efficacy of etrasimod, symptomatic remission, endoscopic improvement, corticosteroid-free remission, and mucosal healing in these participants at time points up to 52 weeks of treatment.

About Ulcerative Colitis

UC is a chronic and often debilitating inflammatory bowel disease[i]  that affects many people worldwide, including an estimated 3.8 million people in North America and Europe.[ii]  Symptoms of UC can include chronic diarrhea with blood and mucus, abdominal pain and cramping, and weight loss. [iii]  UC can have a significant effect on work, family and social activities.[iv]

About Everest Medicines

Everest Medicines is a biopharmaceutical company focused on developing and commercializing transformative pharmaceutical products that address critical unmet medical needs for patients in Asian markets. The management team of Everest Medicines has deep expertise and an extensive track record of high-quality clinical development, regulatory affairs, CMC, business development and operations both in China and with leading global pharmaceutical companies. Everest Medicines has built a portfolio of eleven potentially global first-in-class or best-in-class molecules, many of which are in late-stage clinical development. The Company's therapeutic areas of interest include oncology, autoimmune disorders, cardio-renal diseases and infectious diseases. For more information, please visit its website at www.everestmedicines.com.

Forward-Looking Statements:

This news release may make statements that constitute forward-looking statements, including descriptions regarding the intent, belief or current expectations of the Company or its officers with respect to the business operations and financial condition of the Company, which can be identified by terminology such as "will," "expects," "anticipates," "future," "intends," "plans," "believes," "estimates," "confident" and similar statements. Such forward-looking statements are not guarantees of future performance and involve risks and uncertainties, or other factors, some of which are beyond the control of the Company and are unforeseeable. Therefore, the actual results may differ from those in the forward-looking statements as a result of various factors and assumptions, such as future changes and developments in our business, competitive environment, political, economic, legal and social conditions. The Company or any of its affiliates, directors, officers, advisors or representatives has no obligation and does not undertake to revise forward-looking statements to reflect new information, future events or circumstances after the date of this news release, except as required by law.

[i]   Crohn's and Colitis Foundation. What is Ulcerative Colitis. Available at:  What is Ulcerative Colitis? | Crohn's & Colitis Foundation (crohnscolitisfoundation.org) Accessed March 18, 2022.

[ii] Seyedian, SS.  A review of the diagnosis, prevention, and treatment methods of inflammatory bowel disease.  J Med Life 2019 Apr-Jun; 12 (2):  113-122.  Available at: A review of the diagnosis, prevention, and treatment methods of inflammatory bowel disease - PMC (nih.gov). Accessed March 22, 2022.

[iii] Hanauer SB. Inflammatory bowel disease. N Engl J Med. 1996;334(13):841-8.  Available at:  Inflammatory Bowel Disease | NEJM.  Accessed March 18, 2022.

[iv] Irvine EJ. Quality of Life of Patients with Ulcerative Colitis: Past, Present, and Future. Inflammatory Bowel Diseases. 2008;14(4):554-563.  Available at:  Quality of life of patients with ulcerative colitis: Past, present, and future | Inflammatory Bowel Diseases | Oxford Academic (openathens.net).  Accessed March 18, 2022.

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SOURCE Everest Medicines

FAQ

What are the results of the Phase 3 ELEVATE UC 52 trial for etrasimod?

The Phase 3 ELEVATE UC 52 trial reported significant improvements in clinical remission for etrasimod at 12 and 52 weeks compared to placebo.

What is the regulatory status of etrasimod?

Pfizer expects to initiate regulatory filings for etrasimod later this year.

How many patients were enrolled in the ELEVATE UC 52 trial?

The ELEVATE UC 52 trial enrolled 433 patients with moderately to severely active ulcerative colitis.

What is the significance of the ELEVATE UC 52 trial results for the market?

The trial results suggest etrasimod could be a best-in-class therapy for ulcerative colitis, potentially impacting Pfizer's market position.

What is the safety profile of etrasimod based on recent studies?

Etrasimod demonstrated a safety profile consistent with previous studies, including the Phase 2 OASIS trial.

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