Core Insights - Recursion announced preliminary safety and efficacy results from its Phase 1b/2 TUPELO trial of REC-4881, an investigational MEK1/2 inhibitor for Familial Adenomatous Polyposis (FAP) [1][5] Company Overview - Recursion is a clinical-stage TechBio company focused on decoding biology to improve lives, utilizing its Recursion OS platform to analyze biological and chemical datasets [23] - The company has received Fast Track and Orphan Drug designations from the U.S. FDA for REC-4881, which is aimed at treating FAP, a rare inherited disorder [2] Clinical Trial Details - The TUPELO trial is evaluating the safety, tolerability, pharmacokinetics, and preliminary efficacy of REC-4881 in patients with FAP [6][8] - The Phase 1b portion was a randomized, double-blind, placebo-controlled safety run-in, while the ongoing Phase 2 portion is open-label [7][8] Efficacy Results - As of March 17, 2025, REC-4881 treatment led to a preliminary median 43% reduction in polyp burden at Week 13 among six efficacy-evaluable patients [3][10] - Five out of six patients (83%) experienced reductions in polyp burden ranging from 31% to 82%, while one patient showed a 595% increase from baseline [3][10] - Three of six patients (50%) achieved a ≥1-point reduction in Spigelman stage, indicating improvement in disease severity [11] Safety Profile - Among 19 safety-evaluable patients, 79% experienced at least one treatment-related adverse event (TRAE), with the majority being Grade 1 or 2 [4][16] - The most frequent TRAEs included acneiform rash, diarrhea, and decreased left ventricular ejection fraction (LVEF) [4][17] - Grade 3 TRAEs occurred in 16% of patients, with no Grade ≥4 events reported [4][18] Next Steps - Patient enrollment in the TUPELO trial is ongoing, with additional efficacy and safety analyses anticipated in the second half of 2025 [21]

Nautilus Biotechnology (NAUT) Q1 2025 Earnings Call April 29, 2025 08:30 AM ET Company Participants Ji-Yon Yi - Vice PresidentSujal Patel - Co-Founder, CEO & DirectorParag Mallick - Co-Founder, Chief Scientist & DirectorAnna Mowry - Chief Financial OfficerElizabeth Koslosky - Global Investment Research AssociateThomas VonDerVellen - Equity Research Associate Conference Call Participants Jason Lai - Analyst Operator Good day, and thank you for standing by. Welcome to the Nautilus First Quarter twenty twenty ...

Nurix’s DEL-AI platform uses a first-in-class DEL Foundation Model trained on the Company’s proprietary DNA encoded library data Nurix’s DEL Foundation Model can accurately predict novel binders to therapeutically relevant targets, including many targets considered undruggable, with the potential to accelerate the discovery of novel drugs SAN FRANCISCO, April 28, 2025 (GLOBE NEWSWIRE) -- Nurix Therapeutics, Inc. (Nasdaq: NRIX), a clinical-stage biopharmaceutical company focused on the discovery, developmen ...

Core Insights - Recursion is set to present preliminary data from its Phase 1b/2 clinical trial, TUPELO, evaluating the safety and preliminary activity of REC-4881 for treating familial adenomatous polyposis (FAP) at the 2025 Digestive Disease Week meeting [1][2] - FAP is a rare hereditary condition affecting approximately 50,000 individuals across the US and Europe, with no FDA-approved therapies currently available [2][4] - REC-4881 is a non-ATP-competitive allosteric small molecule MEK 1/2 inhibitor identified through Recursion's AI-powered platform [3][4] Clinical Trial Details - The TUPELO trial is a multicenter, open-label study assessing REC-4881's efficacy, safety, and pharmacokinetics in patients with FAP post-colectomy/proctocolectomy [5] - As of February 7, 2025, 13 patients received 4 mg of REC-4881 daily, with 84.6% experiencing at least one treatment-related adverse event, primarily mild rashes [4] - Among 5 efficacy-evaluable patients, there was a greater than 30% median reduction in total polyp burden after 12 weeks of treatment [4] Upcoming Presentation - The presentation titled "Ongoing Phase 1b/2 Trial of the Allosteric MEK1/2 Inhibitor REC-4881 as Monotherapy in Familial Adenomatous Polyposis (FAP): Preliminary Safety and Efficacy Data" is scheduled for May 4, 2025, from 9:15 AM to 9:30 AM PDT [5] Company Overview - Recursion is a clinical stage TechBio company focused on decoding biology to improve lives, utilizing its Recursion OS platform to analyze vast biological and chemical datasets [7][8] - The company operates one of the most powerful supercomputers globally, enabling extensive experimental and computational capabilities [8] - Recursion is headquartered in Salt Lake City and has multiple offices across North America and Europe [9]

Core Viewpoint - Cassava Sciences, Inc. announces the retirement of Chief Medical Officer James W. Kupiec, MD, effective May 9, 2025, and the appointment of Jack Moore, PhD, as Senior Vice President of Clinical Development, effective April 28, 2025, to advance the clinical evaluation of simufilam for CNS disorders, including TSC-related epilepsy [1][3][8] Company Leadership Changes - James W. Kupiec, MD, retires after a notable career in Alzheimer's disease drug development, contributing to high-quality clinical trials at Cassava [2] - Jack Moore, PhD, brings extensive experience in CNS drug development and will focus on advancing simufilam in new indications [3][4] Clinical Development Focus - Dr. Moore will be responsible for the clinical evaluation of simufilam, targeting TSC-related epilepsy and exploring additional applications [3][5] - The company aims to identify potential clinical collaborators and study sites as part of its strategy for the TSC program [4] Background of Jack Moore - Jack Moore has a strong background in biopharmaceuticals, with experience in CNS and neurodegenerative diseases, having held leadership roles at major pharmaceutical companies [6] - He holds a PhD in Neuroscience and has a history of engaging with key opinion leaders and patient advocacy groups [7] Company Overview - Cassava Sciences, Inc. is a clinical-stage biotechnology company focused on developing investigational treatments for CNS disorders, including simufilam, which targets the filamin A protein [8]

While the impact of unanticipated tariff policy changes in early April was market-wide, the recovery has been less even. Despite a major rebound following the sell-off, some firms have been sluggish to reclaim lost ground. This has given faster-moving stocks an opportunity to stand out as fresh momentum plays in the meantime. Investors looking for high-momentum stocks following this period of turbulence should consider whether the factors are short-term or indicative of potentially longer-term trajectories. ...

Core Insights - REC-3565 is a promising MALT1 inhibitor aimed at treating relapsed or refractory B-cell lymphomas, with the first patient dosed in the Phase 1 EXCELERIZE clinical study [1][2] - The drug is designed to minimize the risk of hyperbilirubinemia, a common side effect associated with other MALT1 inhibitors, enhancing its safety profile [1][3] - The EXCELERIZE study will evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and preliminary efficacy of REC-3565 in two parts, focusing on both monotherapy and combination therapies [2][3] Company Overview - Recursion is a clinical stage TechBio company that utilizes AI-driven approaches to enhance drug discovery, operating one of the largest proprietary biological and chemical datasets [4] - The company is headquartered in Salt Lake City and is a founding member of BioHive, a collective for the Utah life sciences industry [5] Market Potential - Approximately 41,000 relapsed and/or refractory patients with chronic lymphocytic leukemia (CLL) and B-cell lymphomas in the U.S. and EU5 are eligible for treatment annually, indicating a significant market opportunity for REC-3565 [3]

Core Insights - Kanvas Biosciences has introduced its High-Phylogenetic-Resolution Spatial Mapping (HiPR-Map) Platform, which significantly outperforms conventional sequencing methods, achieving a sensitivity of 0.01% for species-level microbial identification [1][4]. Group 1: Technology and Capabilities - The HiPR-Map Platform utilizes advanced spectral imaging technology to enable precise enumeration and spatial localization of microbial cells within complex communities, particularly excelling in low biomass environments [1][4]. - HiPR-Map can detect single nucleotide polymorphisms (SNPs) in the 16S rRNA sequence, allowing for species-level microbial identification and achieving superior sensitivity compared to traditional sequencing methods [6]. - The platform provides comprehensive insights into microbial interactions, which are essential for optimizing live biotherapeutic products (LBPs) [3][4]. Group 2: Applications in Biotherapeutics - LBPs represent a significant advancement over traditional fecal microbiota transplants (FMTs) in treating diseases such as colitis and various cancers, necessitating a deeper understanding of microbial interactions beyond mere identification [3]. - Kanvas' HiPR-Map technology enhances the therapeutic potential of LBPs by allowing for precise manipulation and optimization based on detailed microbial interaction data [3][4]. - The platform has demonstrated the ability to reveal host-microbiome-food interactions and microbial enrichment patterns, which are critical for LBP manufacturing and therapeutic evaluation [6]. Group 3: Research Findings - The recent research paper highlights three key findings: 1. Superior technical strengths of HiPR-Map in comparison to sequencing methods [6]. 2. Engraftment profiles of Kanvas LBPs in the mouse gastrointestinal tract, revealing important interactions [6]. 3. Spatial interactions of microbes at microscale and mesoscale, providing insights that are vital for LBP development [6]. Group 4: Company Overview - Kanvas Biosciences is focused on building a microbiome drug screening, discovery, and manufacturing platform aimed at accelerating the development of next-generation live biotherapeutics [9]. - The company is headquartered in Princeton, NJ, and has received investments from notable firms, positioning it uniquely in the market for developing therapeutics that improve microbiome health [9].

Recursion (NASDAQ: RXRX) is a clinical stage TechBio company leading the space by decoding biology to radically improve lives. Enabling its mission is the Recursion OS, a platform built across diverse technologies that continuously generate one of the world's largest proprietary biological and chemical datasets. Recursion leverages sophisticated machine-learning algorithms to distill from its dataset a collection of trillions of searchable relationships across biology and chemistry unconstrained by human bi ...

The funding will accelerate further development of Isomorphic's AI drug design engine and support the company's goal of bringing its discovered drugs to clinical trials. Isomorphic Labs was founded by DeepMind co-founder Demis Hassabis by leveraging DeepMind's software for AI drug discovery, including AlphaFold, an AI model that predicts the three-dimensional structures of proteins. Last year, Isomorphic Labs secured strategic partnerships with Eli Lilly and Novartis, potentially generating up to $3 billion ...