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(MENAFN - African Press Organization)CAIRO, Egypt, January 23, 2026/APO Group/ --African Export-Import Bank (Afreximbank) ( ) has been registered with the ISO 31000:2018 Risk Management Standard ...
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Press Release: Sanofi's amlitelimab confirms its potential in atopic dermatitis Stocks master_of_puppetsFri 23/01/2026 - 07:00 FR0000120578 FR0000120578 FR0000120578 23/01/2026 - 07:00 Paris Press Release: Sanofi's amlitelimab confirms its potential in atopic dermatitis Other subject 1001160718-en GlobeNewswire Sanofi Winthrop Industrie Euronext Published 20103015 Pharmaceuticals XPAR BGEM ETLX Language English Sanofi's amlitelimab confirms its potential in atopic dermatitis In the SHORE phase 3 study, amlitelimab in combination with topical therapies met all primary and key secondary endpoints at Week 24 with efficacy progressively increasing throughout the treatment period with some patients improving as early as Week 2In the COAST 2 phase 3 study, amlitelimab demonstrated statistically significant efficacy on vIGA-AD 0/1, the primary endpoint as assessed for the US and US reference countries, and confirmed COAST 1 potential for Q12W dosing from the start; amlitelimab did not achieve statistical significance for the co-primary endpoints as assessed for the EU and EU reference countriesBased on the totality of data, Sanofi will move forward with global regulatory submissions for amlitelimabA preliminary analysis of the ATLANTIS phase 2 study showed continued and progressive improvements with no evidence of plateau through Week 52, demonstrating the potential of OX40-ligand as an important new mechanism in AD Paris, January 23, 2026. Following the positive COAST 1 (clinical study identifier: https://www.clinicaltrials.gov/study/NCT06130566?term=NCT06130566&rank=...; rel="nofollow" target="_blank">NCT06130566) results in September 2025, two additional global phase 3 studies – SHORE (clinical study identifier: https://clinicaltrials.gov/study/NCT06224348?term=NCT06224348&rank=1&qu...; rel="nofollow" target="_blank">NCT06224348) and COAST 2 (clinical study identifier: https://clinicaltrials.gov/study/NCT06181435" rel="nofollow" target="_blank">NCT06181435) – of amlitelimab, a fully human non-T cell depleting monoclonal antibody that selectively targets OX40-ligand (OX40L), today delivered a robust body of evidence that supports amlitelimab’s potential in the treatment of patients 12 years and older with moderate-to-severe atopic dermatitis (AD). In these two phase 3 studies amlitelimab was well-tolerated and the safety profile was consistent with previously reported data. "Importantly, these results validate amlitelimab’s novel mechanism of action to block OX40-ligand without T-cell depletion and its promise to normalize the immune system over time," said Houman Ashrafian, Executive Vice President, Head of Research & Development at Sanofi. "The totality of data seen to date reinforce our confidence in amlitelimab’s potential to deliver both Q12W dosing from the start and progressive efficacy through Week 52. We look forward to sharing additional results, including longer-term data, as we move toward global regulatory submissions.” For both SHORE and COAST 2 phase 3 studies, key endpoints were measured at Week 24 in patients aged 12 years and older with moderate-to-severe AD who received amlitelimab either every four weeks (Q4W) or every 12 weeks (Q12W). For US and US reference countries, the single primary endpoint was the proportion of patients with a validated investigator global assessment scale for AD (vIGA-AD) of 0 (clear) or 1 (almost clear) and a reduction from baseline score of ≥2 points, analyzed using non-responder imputation (US estimand). For the EU, EU reference countries and Japan, the co-primary endpoints comprised the proportion of patients with vIGA-AD 0/1 and a reduction from baseline score of ≥2 points along with the proportion of patients reaching a 75% or greater improvement in the eczema area and severity index total score (EASI-75), both analyzed using treatment policy (EU estimand). SHORE studyIn the SHORE study, amlitelimab, dosed either Q4W or Q12W in conjunction with medium-potency background topical corticosteroids (TCS) with or without topical calcineurin inhibitors (TCI), met all primary and key secondary endpoints compared to placebo plus TCS with or without TCI at Week 24, across both US and EU estimands. SHORE primary endpointsKey endpointsProportion of patientsNon-responder imputation*+(US estimand)Treatment policy**+(EU estimand) Q4WQ12WPlaceboQ4WQ12WPlacebovIGA-AD 0/128.7%p-value (p)p≤0.01 32.3%p ≤0.0116.8% 29.9%p≤0.0132.9%p≤0.0116.8% EASI-7548.1%p≤0.0146.8%p≤0.02532.3% 50.9%p≤0.00148.1%p≤0.02534.2% * Non-responder imputation (NRI): patients with rescue or prohibited medication use before Week 24 or with missing efficacy assessments at Week 24 are classified as non-responders. ** Treatment policy: all data are included regardless of rescue medication use prior to Week 24. Patients with prohibited medication use before Week 24 or with missing efficacy assessments at Week 24 are classified as non-responders.+ Statistical analyses followed a pre‐specified hierarchical testing procedure to control for multiplicity. For the pre-specified endpoints across the two doses, the statistical significance level was adjusted (alpha‐split) to two-sided p.025. COAST 2 studyIn the COAST 2 study, amlitelimab monotherapy dosed either Q4W or Q12W met the primary endpoint of the proportion of patients achieving vIGA-AD 0/1 and a reduction from baseline score of ≥2 points compared to placebo at Week 24, as assessed for the US and US reference countries. The key secondary endpoint of the proportion of patients who achieved vIGA-AD 0/1 with barely perceptible erythema (BPE), as assessed for the US and US reference countries, did not achieve statistical significance. For the EU and EU reference countries, amlitelimab dosed either Q4W or Q12W did not achieve statistical significance for the co-primary endpoints of proportion of patients achieving vIGA-AD 0/1 and EASI-75 compared to placebo. Therefore, in accordance with hierarchical statistical testing procedures, p-values presented below for additional secondary endpoints reflect nominal significance without adjustment for multiplicity. COAST 2 primary endpointsKey endpointsProportion of patientsNon-responder imputation*+(US estimand)Treatment policy**+(EU estimand) Q4WQ12WPlaceboQ4WQ12WPlacebovIGA-AD 0/125.3%p≤0.025 25.7%p≤0.02514.8%28.8%p=0.03127.7%p=0.06818.8%EASI-7541.8%p≤0.001***40.5%p≤0.01***24.2%49.7%p≤0.001***45.9%p≤0.01***30.2% * Non-responder imputation (NRI): patients with rescue or prohibited medication use before Week 24 or with missing efficacy assessments at Week 24 are classified as non-responders.** Treatment policy: all data are included regardless of rescue medication use prior to Week 24. Patients with prohibited medication use before Week 24 or with missing efficacy assessments at Week 24 are classified as non-responders.+ Statistical analyses followed a pre‐specified hierarchical testing procedure to control for multiplicity. For the pre-specified endpoints across the two doses, the statistical significance level was adjusted (alpha‐split) to two-sided p < 0.025. Nominal p-values e also reported.*** P-values are nominal without multiplicity adjustment. The most common treatment-emergent adverse events (TEAEs) in SHORE (≥5% in any dose arm; pooled amlitelimab vs. placebo) were nasopharyngitis (9.5% vs 12.5%), upper respiratory tract infection (7.9% vs 4.4%), dermatitis atopic (2.7% vs 5.6%). Overall, rates of TEAEs, serious adverse events, and TEAEs resulting in treatment discontinuation were similar in the pooled amlitelimab arms and placebo arm. The most common TEAEs in COAST 2 (≥5% in any dose arm; pooled amlitelimab vs. placebo) were nasopharyngitis (5.9% vs 7.4%), upper respiratory tract infection (4.8% vs 4.0%), dermatitis atopic (5.3% vs 2.7%). Overall, rates of TEAEs, serious adverse events, and TEAEs resulting in treatment discontinuation were similar in the pooled amlitelimab and placebo arms. Preliminary analysis from ATLANTIS phase 2 open-label studyIn addition, a preliminary analysis of the ongoing, open-label ATLANTIS phase 2 study (clinical study identifier: https://www.clinicaltrials.gov/study/NCT05769777?term=atlantis&intr=Aml...; rel="nofollow" target="_blank">NCT05769777) indicated that amlitelimab dosed Q4W progressively improved skin clearance and disease severity beyond Week 24 to Week 52 in 591 patients aged 12 years and older with moderate-to-severe AD. In this preliminary analysis, amlitelimab was well-tolerated through Week 52. ATLANTIS preliminary analysisKey endpointsProportion of patients Week 24Week 52vIGA-AD 0/1 35.4%50.3%EASI-7562.9%76.5% Patients with missing data are classified as non-responders. Concomitant use of TCS with or without TCI is allowed as needed2. Short-term ( The most common TEAEs in this preliminary analysis of ATLANTIS (≥5%) were nasopharyngitis (19.1%), headache (10.3%), influenza (9.1%), dermatitis atopic (8.6%), upper respiratory tract infection (7.2%) and accidental overdose (5.1%, due to dose scheduling). Serious TEAEs and TEAEs resulting in treatment discontinuation at Week 52 were low, 4.7% and 2.9% respectively. In addition, an event of Kaposi’s sarcoma, determined to be cutaneous, was reported in a patient with known risk factors. The patient stopped amlitelimab and is in the recovery phase. Results for COAST 1, COAST 2, SHORE, and this preliminary analysis of ATLANTIS will be presented at forthcoming medical congresses. Two additional phase 3 studies, AQUA (clinical study identifier: https://clinicaltrials.gov/study/NCT06241118?term=NCT06241118&rank=1&qu...; rel="nofollow" target="_blank">NCT06241118) and ESTUARY (clinical study identifier: https://clinicaltrials.gov/study/NCT06407934?term=NCT06407934&rank=1&qu...; rel="nofollow" target="_blank">NCT06407934) are anticipated to report results in H2 2026. Global regulatory submissions are planned for H2 2026, unchanged. Amlitelimab is currently in clinical development, and its safety and efficacy have not been evaluated by any regulatory authority. About the SHORE studySHORE was a randomized, double-blind, placebo-controlled, parallel-group, 3-arm, multinational, multicenter phase 3 study to evaluate the efficacy and safety of amlitelimab in combination TCS with or without TCI in 596 participants aged 12 years and older with moderate-to-severe AD. Key objectives include measuring the efficacy and safety of amlitelimab compared to placebo at Week 24 when used in combination with TCS/TCI. In the study, amlitelimab was administered at a dose of 250 mg (125 mg for those with body weight About the COAST 2 studyCOAST 2 was a randomized, double-blind, placebo-controlled, parallel-group, 3-arm, global, multicenter phase 3 study to evaluate the efficacy and safety of amlitelimab monotherapy in 547 adults and adolescents aged 12 years and older with moderate-to-severe AD. Key objectives included measuring the efficacy and safety of amlitelimab compared to placebo at Week 24. In the study, amlitelimab was administered at a dose of 250 mg (125 mg for those with body weight About the ATLANTIS studyATLANTIS is a phase 2 global, single-arm, open-label, long-term safety study of amlitelimab for the treatment of patients 12 years or older with moderate to severe atopic dermatitis (AD) with a duration of up to 268 weeks. In the study, patients received weight-based amlitelimab Q4W (250 mg [125 mg for those with body weight About amlitelimabAmlitelimab (SAR445229, KY1005) is a fully human, non-T cell depleting monoclonal antibody that blocks the OX40L, a key immune regulator. With its novel mechanism of action, amlitelimab selectively blocks OX40L signaling during the inflammatory prequel, the initiating phase of an overactive immune system, to potentially normalize T-cell-mediated inflammation without T-cell depletion. About Sanofi Sanofi is an R&D driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. We apply our deep understanding of the immune system to invent medicines and vaccines that treat and protect millions of people around the world, with an innovative pipeline that could benefit millions more. Our team is guided by one purpose: we chase the miracles of science to improve people’s lives; this inspires us to drive progress and deliver positive impact for our people and the communities we serve, by addressing the most urgent healthcare, environmental, and societal challenges of our time.Sanofi is listed on EURONEXT: SAN and NASDAQ: SNY Media RelationsSandrine Guendoul | +33 6 25 09 14 25 | mailto:sandrine.guendoul@sanofi.com" rel="nofollow" target="_blank">sandrine.guendoul@sanofi.comEvan Berland | +1 215 432 0234 | mailto:evan.berland@sanofi.com" rel="nofollow" target="_blank">evan.berland@sanofi.comLéo Le Bourhis | +33 6 75 06 43 81 | mailto:leo.lebourhis@sanofi.com" rel="nofollow" target="_blank">leo.lebourhis@sanofi.comVictor Rouault | +1 617 356 4751 | mailto:victor.rouault@sanofi.com" rel="nofollow" target="_blank">victor.rouault@sanofi.comTimothy Gilbert | +1 516 521 2929 | mailto:timothy.gilbert@sanofi.com" rel="nofollow" target="_blank">timothy.gilbert@sanofi.comLéa Ubaldi | +33 6 30 19 66 46 | mailto:lea.ubaldi@sanofi.com" rel="nofollow" target="_blank">lea.ubaldi@sanofi.comEkaterina Pesheva | +1 410 926 6780 | mailto:ekaterina.pesheva@sanofi.com" rel="nofollow" target="_blank">ekaterina.pesheva@sanofi.com Investor RelationsThomas Kudsk Larsen | +44 7545 513 693 | mailto:thomas.larsen@sanofi.com" rel="nofollow" target="_blank">thomas.larsen@sanofi.comAlizé Kaisserian | +33 6 47 04 12 11 | mailto:alize.kaisserian@sanofi.com" rel="nofollow" target="_blank">alize.kaisserian@sanofi.comKeita Browne | +1 781 249 1766 | mailto:keita.browne@sanofi.com" rel="nofollow" target="_blank">keita.browne@sanofi.comNathalie Pham | +33 7 85 93 30 17 | mailto:nathalie.pham@sanofi.com" rel="nofollow" target="_blank">nathalie.pham@sanofi.comThibaud Châtelet | +33 6 80 80 89 90 | mailto:thibaud.chatelet@sanofi.com" rel="nofollow" target="_blank">thibaud.chatelet@sanofi.comYun Li | +33 6 84 00 90 72 | mailto:yun.li3@sanofi.com" rel="nofollow" target="_blank">yun.li3@sanofi.com Sanofi forward-looking statementsThis press release contains forward-looking statements as defined in the Private Securities Litigation Reform Act of 1995, as amended. Forward-looking statements are statements that are not historical facts. These statements include projections and estimates and their underlying assumptions, statements regarding plans, objectives, intentions, and expectations with respect to future financial results, events, operations, services, product development and potential, and statements regarding future performance. Forward-looking statements are generally identified by the words “expects”, “anticipates”, “believes”, “intends”, “estimates”, “plans” and similar expressions. Although Sanofi’s management believes that the expectations reflected in such forward-looking statements are reasonable, investors are cautioned that forward-looking information and statements are subject to various risks and uncertainties, many of which are difficult to predict and generally beyond the control of Sanofi, that could cause actual results and developments to differ materially from those expressed in, or implied or projected by, the forward-looking information and statements. These risks and uncertainties include among other things, the uncertainties inherent in research and development, future clinical data and analysis, including post marketing, decisions by regulatory authorities, such as the FDA or the EMA, regarding whether and when to approve any drug, device or biological application that may be filed for any such product candidates as well as their decisions regarding labelling and other matters that could affect the availability or commercial potential of such product candidates, the fact that product candidates if approved may not be commercially successful, the future approval and commercial success of therapeutic alternatives, Sanofi’s ability to benefit from external growth opportunities, to complete related transactions and/or obtain regulatory clearances, risks associated with intellectual property and any related pending or future litigation and the ultimate outcome of such litigation, trends in exchange rates and prevailing interest rates, volatile economic and market conditions, cost containment initiatives and subsequent changes thereto, and the impact that global crises may have on us, our customers, suppliers, vendors, and other business partners, and the financial condition of any one of them, as well as on our employees and on the global economy as a whole. The risks and uncertainties also include the uncertainties discussed or identified in the public filings with the SEC and the AMF made by Sanofi, including those listed under “Risk Factors” and “Cautionary Statement Regarding Forward-Looking Statements” in Sanofi’s annual report on Form 20-F for the year ended December 31, 2024. Other than as required by applicable law, Sanofi does not undertake any obligation to update or revise any forward-looking information or statements. All trademarks mentioned in this press release are the property of the Sanofi group. Attachment Press_Releasehttps://ml-eu.globenewswire.com/Resource/Download/dc86a594-a982-488d-bd...; https://www.globenewswire.com/newsroom/ti?nf=MTAwMTE2MDcxOCM0MDIzMjA2OD...; /> https://ml-eu.globenewswire.com/media/ZWQ3ZTI3ZTAtMGQyMi00YTkzLWI3N2QtO...; referrerpolicy="no-referrer-when-downgrade" /> SANOFI SANOFI 078526 FR0000120578-XPAR FR0000120578-BGEM FR0000120578-ETLX SAN 1SAN 4SAN
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Bitwise Says Crypto Has Likely Bottomed, Echoing Q1 2023 Setup Bitwise Asset Management is arguing that crypto’s current drawdown has the fingerprints of a cyclical low: weak prices alongside strengthening on-chain and business fundamentals, a pattern the firm says last appeared in Q1 2023 before a multi-year rally. In its Q4 2025 “Crypto Market Review,” [...]
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