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Artiva Biotherapeutics Announces Positive Initial Safety and Translational Data Supporting Deep B-Cell Depletion with AlloNK® in Autoimmune Disease
Globenewswire· 2025-11-12 12:20
Core Insights - Artiva Biotherapeutics announced positive initial safety and translational data from clinical trials of AlloNK in combination with anti-CD20 monoclonal antibodies for autoimmune diseases, indicating that AlloNK is well tolerated and effective in B-cell depletion [2][3] Group 1: Treatment Efficacy and Safety - AlloNK, an allogeneic NK cell therapy, demonstrated consistent and complete B-cell depletion in all patients treated by Day 13, comparable to results seen in B-cell driven lymphoma [1][3] - No cytokine release syndrome (CRS) or immune effector cell-associated neurotoxicity syndrome (ICANS) was reported, and the treatment was generally well tolerated with most adverse events being Grade 1 or 2 [1][10] - Among 32 patients treated, all demonstrated non-quantifiable peripheral CD19+ B-cell levels by Day 13, supporting the intended mechanism of action for AlloNK [10] Group 2: Clinical Trials and Future Plans - Artiva is conducting three ongoing Phase 1 and 2 clinical trials for refractory rheumatoid arthritis (RA), Sjögren's disease, and other autoimmune conditions, with plans to share initial clinical response data in the first half of 2026 [3][10] - The company aims to align with the U.S. Food and Drug Administration (FDA) on pivotal trial design for AlloNK in refractory RA in the first half of 2026 [1][10] Group 3: Market Opportunity - There is a significant unmet need for patients with refractory RA who have failed at least two biologic or targeted synthetic disease-modifying anti-rheumatic drugs (b/ts DMARDs), representing over 150,000 patients in the U.S. [10] - Current real-world data shows only a 10-20% ACR50 response in patients who have failed two or more b/ts DMARDs, indicating room for improvement with AlloNK [10]
Press Release: Sanofi completes acquisition of DR-0201
Globenewswire· 2025-05-27 05:00
Core Viewpoint - Sanofi has completed the acquisition of DR-0201, now named SAR448501, to enhance its immunology pipeline and position itself as a leading immunology company [1][2]. Group 1: Acquisition Details - The acquisition involved an upfront payment of $600 million, with potential future payments totaling $1.3 billion based on development and launch milestones [4]. - Dren Bio will continue to operate independently to advance its pipeline of antibody therapeutics [4]. Group 2: Product Information - SAR448501 is a targeted bispecific myeloid cell engager that has demonstrated robust B-cell depletion in pre-clinical and early clinical studies [2]. - The product targets specific tissue-resident and trafficking myeloid cells to induce deep B-cell depletion through targeted phagocytosis [2]. Group 3: Clinical Implications - Recent studies suggest that deep B-cell depletion may reset the adaptive immune system, potentially leading to sustained treatment-free remission in patients with refractory B-cell mediated autoimmune diseases, such as lupus [3]. - There remains a significant unmet medical need in treating these autoimmune diseases [3].