Abivax reports 2020 financial results and operations update (news with additional features)
/ Key word(s): Annual Results
Abivax reports 2020 financial results and
PARIS, France, March 31, 2021 - 06:00 p.m. (CET) - Abivax SA (Euronext Paris: FR0012333284 - ABVX), a clinical-stage biotechnology company developing novel therapies that modulate the immune system to treat chronic inflammatory diseases, viral infections, and cancer, today announced its 2020 annual financial results, as of December 31, 2020, and provides an update on the progress of its product pipeline. The financial statements for 2020, approved by the Company's Board of Directors on March 30, 2021, have been audited and the certification report is being prepared by the Company's external auditors.
"2020 was a very successful year for Abivax as we substantially advanced the late-stage clinical development for our core clinical program in chronic inflammatory diseases. Abivax reached several important milestones in 2020 despite the challenges of the Covid-19pandemic. We confirmed the long-term safety and efficacy of ABX464 in ulcerative colitis patients in our two-year phase 2a maintenance study. Patient recruitment was completed for the phase 2b study of ABX464 to treat ulcerative colitis in December 2020, and for the phase 2a study in rheumatoid arthritis in February of this year. We look forward to bringing ABX464 into a global phase 3 clinical program in UC later this year. We also plan to initiate execution of a phase 2b/3 study to treat Crohn's disease in 2021, consistent with our development strategy in inflammatory bowel diseases.", said Prof. Hartmut Ehrlich, M.D., CEO of Abivax. "Our second compound, ABX196 for hepatocellular carcinoma, also made progress in phase 1/2 clinical testing in the US. The recruitment of liver cancer patients for the dose escalation phase will be completed shortly and the results will become available in Q2 2021. Although we recently stopped the phase 2b/3 clinical trial with ABX464 in acute Covid-19 for lack of efficacy, the generated data underpin the favorable safety and tolerability profile of ABX464 and are very valuable for our inflammation program. The lack of efficacy of ABX464 in the hyper-acute setting, characterized by cytokine storm and ARDS in severe Covid-19, has no bearing on our IBD program, as the molecule has clearly demonstrated efficacy and safety in controlling chronic intestinal inflammation. Abivax is looking forward to establishing ABX464 as a novel, safe and well-tolerated oral long-term treatment option for the many patients suffering from chronic inflammatory diseases."
Didier Blondel, CFO of Abivax, added: "Abivax successfully secured EUR 84M major financing in 2020. With our current and available cash resources, our operations are fully funded through Q4 2021. In the months to come, Abivax will focus on advancing its clinical late-stage core program with ABX464 in ulcerative colitis, Crohn's disease as well as rheumatoid arthritis. The expected clinical read-outs in Q2 2021, will give us more visibility on the strategic possibilities for the Company and we will carefully evaluate and select the most attractive options to create shareholder value. Our priority remains partnering with a large pharma or biotech company in the short term, once the UC phase 2b data are available."
ABX464 in ulcerative colitis (UC)
Abivax reported excellent two-year safety and efficacy data from the ABX464 UC phase 2a maintenance study in September 2020. These results confirmed the good safety profile and durable efficacy of 50 mg once-daily oral ABX464 in patients with moderate-to-severe UC. After the second year of treatment, 69% of patients were in clinical remission and 94% benefited from a clinical response. Furthermore, blinded readings of the endoscopies were performed centrally by independent reviewers. Median fecal calprotectin, the key biological marker of UC disease activity, remained at 31.6 µg/g (normal levels are below 50 µg/g).
Abivax's phase 2b study with ABX464, ABX464-103, in patients with moderate-to-severe UC is ongoing. The recruitment of 254 patients within the induction study was achieved in December 2020. Patients who completed the ABX464-103 trial had the option to continue their treatment in the corresponding open-label maintenance study ABX464-104 for up to two years to confirm the long-term safety and efficacy profile of ABX464. The phase 2b induction and maintenance studies are conducted in over 130 study centers in 15 European countries, Canada and the US. Top-line results after the induction treatment will become available in Q2 2021.
At present, more than 800 patients have been treated with ABX464 across different indications, including UC patients, some of whom are in their fourth year of continuous daily dosing.
To date, once daily oral ABX464 has a very good clinical safety and tolerability profile including evidence of short- and long-term efficacy in the treatment of UC patients. Abivax is preparing to start its clinical phase 3 program in UC by year end.
ABX464 in rheumatoid arthritis (RA)
The recruitment of 60 patients in the ABX464-301 phase 2a study in moderate-to-severe active RA was achieved in February 2021. Patients who completed the induction study could transition to the one-year open-label maintenance study, ABX464-302, to evaluate the long-term safety and efficacy of ABX464 in RA.
The phase 2a study is designed to evaluate the safety, tolerability, and preliminary efficacy of two oral dose-levels of ABX464 administered daily, in combination with methotrexate (MTX), for RA patients who had an inadequate response to either MTX and/or anti-tumor necrosis factor alpha (TNFα) biological therapeutics. The trial is being conducted in 24 study centers across five European countries. Top-line data after 3 months of induction treatment will become available in Q2 2021.
Abivax is preparing to start a clinical phase 2b program in RA in early 2022.
ABX464 in Crohn's disease (CD)
Following the very promising results of the phase 2a induction and maintenance studies in UC, Abivax's IBD steering committee recommended skipping a phase 2a proof-of-concept study in CD, due to the pathophysiological and clinical similarities of CD and UC. Abivax is planning to directly initiate a phase 2b/3 study in CD with the objective to demonstrate a similar strong efficacy and favorable safety as already reported in UC. The inclusion of the first patient into this study is planned for the second half of 2021.
ABX464 market potential in inflammatory diseases
The inflammatory disease space represents an area of high unmet medical need, and a corresponding substantial market opportunity. According to recent statistics, there were an estimated 3.5M diagnosed cases of UC in G7 countries (US, France, Germany, Italy, Spain, UK and Japan) in 2020. This represents a potential market opportunity of up to USD 6.2B annually, based on 2020 pharmaceutical sales estimates in these countries for UC only. For IBD (UC and CD), these sales have reached about USD 17.7B in 2020 and are estimated to grow to USD 24.4B in 2025, i.e. the year ABX464 is expected to reach the market. There were approximately 3.8M diagnosed cases of RA in G7 countries in 2020, representing a market potential of about USD 20.2B.
The market potential for the full range of inflammatory conditions (including neuro-inflammatory diseases) is currently estimated to be in excess of USD 90B.
Abivax's mission for ABX464 is to offer a new therapeutic option to patients suffering from chronic inflammatory diseases with improved short- and long-term efficacy and good safety.
Abivax's strategy is to develop ABX464 in inflammatory bowel diseases (UC and CD) and expand the clinical program to further chronic inflammatory indications, including RA.
ABX464 has the potential to take a substantial commercial market share in the IBD field.
ABX196 in hepatocellular carcinoma (HCC)
The phase 1/2 clinical trial in HCC is ongoing at the Scripps MD Anderson Cancer Center in San Diego and the MD Anderson Cancer Center in Houston. In this proof-of-concept study, patients who are failing on checkpoint inhibitors are treated with ABX196 in combination with nivolumab (Opdivo(R), Bristol Myers Squibb). The clinical study consists of two phases, a dose escalation phase, and a subsequent expansion phase.
The patient recruitment within the dose escalation phase will be completed shortly, with top-line data in Q2 2021. The most efficient and well-tolerated dose of ABX196 will be defined and applied to the follow-on expansion phase, to be started in Q3 2021.
Stopping of ABX464 in Covid-19 - miR-AGE trial
On March 5, 2021, Abivax announced it would be stopping the phase 2b/3 Covid-19 study (miR-AGE trial - ABX464-401) due to lack of efficacy. This decision followed the recommendation of the Data Safety and Monitoring Board (DSMB), based on an interim analysis evaluating data of 305 high-risk Covid-19 patients after they completed the 28-days study period.
This press release contains forward-looking statements, forecasts and estimates (including patient recruitment) with respect to certain of the Company's programs. Although the Company believes that its forward-looking statements, forecasts and estimates are based on assumptions and assessments of known and unknown risks, uncertainties and other factors that have been deemed reasonable, such forward-looking statements, forecasts and estimates are subject to a number of risks and uncertainties that could cause actual results to differ materially from those anticipated in such forward-looking statements, forecasts and estimates. A description of these risks, contingencies and uncertainties can be found in the documents filed by the Company with the French Autorité des Marchés Financiers pursuant to its legal obligations including its registration document (Document d'Enregistrement Universel). Furthermore, these forward-looking statements, forecasts and estimates are only as of the date of this press release. Readers are cautioned not to place undue reliance on these forward-looking statements. Abivax disclaims any obligation to update these forward-looking statements, forecasts or estimates to reflect any subsequent changes that the Company becomes aware of, except as required by law.
 Vermeire S, Hébuterne X, Tilg H, De Hertogh G, Gineste P, Steens J-M, on behalf on the ABX464 Investigators, Induction and long-term follow-up with ABX464 for moderate-tosevere ulcerative colitis: Results of phase 2a trial, Gastroenterology (2021), doi: https://doi.org/10.1053/ j.gastro.2021.02.054.
File: Abivax Pipeline
31.03.2021 Dissemination of a Corporate News, transmitted by DGAP - a service of EQS Group AG.