1. Foghorn and Lilly stop advancing FHD-9091
Foghorn Therapeutics said on 1 October that it and Lilly would not advance the SMARCA2 inhibitor FHD-909 into trial expansion after Phase 1 dose escalation. The company attributed the decision to insufficient efficacy despite target inhibition and drug exposures that met its preclinical expectations. It also stopped a separate SMARCA2 degrader programme and announced a workforce reduction of about 40%. Foghorn will prioritise other programmes, including EP300 and oral immunology. The decision changes a prominent chromatin-targeted development effort; the announcement does not establish that every way of targeting SMARCA2 will fail.1
2. Wave outlines a registration plan for RNA editing in AATD2
Wave Life Sciences reported FDA agreement on key elements of a planned registration pathway for WVE-006, its investigational RNA-editing treatment for alpha-1 antitrypsin deficiency. The company plans a single two-year trial to support potential full approval, with a one-year interim analysis that could support accelerated approval using disease biomarkers. Wave also said the agency supported its mass-spectrometry assay for measuring wild-type and mutant alpha-1 antitrypsin proteins. The announcement connects an emerging RNA-editing modality with a proposed regulatory and measurement strategy. It reports the company’s account of discussions, rather than an approval or a new demonstration of clinical benefit.2
3. Datroway collaboration plans a new breast-cancer combination trial3
AstraZeneca and Daiichi Sankyo announced a clinical-trial collaboration with Summit Therapeutics to test Datroway with ivonescimab in lung and breast cancers. The partners intend to begin a Phase III study in previously untreated triple-negative breast cancer, pairing a TROP2-directed antibody–drug conjugate with a bispecific immunotherapy. Under the agreement, AstraZeneca or Daiichi Sankyo will sponsor trials, while the companies supply their medicines and share development costs. For medicinal-chemistry and pharmacology teams, the agreement specifies a combination and clinical setting for testing how these treatment approaches work together. The October announcement describes planned studies, with no combination efficacy results.3
4. DOE opens a broad basic-research funding call4
The US Department of Energy announced up to $400 million for its annual basic-research funding call, spanning seven Office of Science programmes. The scope includes Basic Energy Sciences, advanced scientific computing, and biological and environmental research, making the opportunity relevant across chemical research and computational methods. The FY2027 solicitation was posted on 30 September, ahead of the 1 October announcement, and accepts applications through September 2027 unless superseded. Programme-specific review and preapplication arrangements still apply.5 This is an opportunity to compete for support, rather than an allocation of $400 million to projects already selected.4
5. DeepMind releases tools for tracing AI-designed proteins6
Google DeepMind announced SynthID Bio on 30 September, making code and laboratory data available and releasing model weights to researchers. The tools embed detectable signatures in generated protein sequences or predicted structures. The official repository includes a ProteinMPNN-based sequence workflow and points to instructions for using watermarked AlphaFold 3 predictions.7 This gives research teams an implementation to evaluate biological-design provenance within their own workflows. DeepMind describes the work as a proof of concept: wider use still needs research and community coordination, including stronger resistance to deliberate watermark removal.6
References
Foghorn Therapeutics. Foghorn Therapeutics Provides Update on FHD-909 and Strategic Priorities. Company announcement via GlobeNewswire; 2026; Official announcement. Accessed 2026-10-04T16:17:47.867Z.
Source evidence and access
Opening; strategic priorities; CEO explanation
FHD-909 Phase1 dose escalation completed; Foghorn and Lilly will not advance expansion. CEO attributes decision to insufficient efficacy despite selective SMARCA2 target inhibition, favorable safety and achieved exposures. Separate SMARCA2 degrader stopped; about40% staff reduction; prioritize EP300, oral immunology, CBP and induced proximity.
Full responsible original announcement inspected in web source reader; agency register inspected for original call date.
Wave Life Sciences. Wave Life Sciences Announces FDA Feedback Supports Registrational Pathway for WVE-006 (RNA Editing) in AATD. Company investor announcement; 2026; Official announcement. Accessed 2026-10-04T16:17:47.867Z.
Source evidence and access
Opening and planned registrational strategy
Company reports FDA alignment on key elements WVE-006 registration strategy. Planned single two-year trial for full approval with one-year interim analysis for potential accelerated approval. Biomarker strategy includes LC-MS wild-type M-AAT and mutant Z-AAT. Not an approval or efficacy result.
Full responsible original announcement inspected in web source reader; agency register inspected for original call date.
AstraZeneca and Daiichi Sankyo. AstraZeneca and Daiichi Sankyo announce clinical collaboration with Summit Therapeutics to evaluate Datroway in combination with ivonescimab across multiple tumour types. Company announcement; 2026; Official announcement. Accessed 2026-10-04T16:17:47.867Z.
Source evidence and access
Opening; Phase III plan; agreement terms
Datroway plus ivonescimab across lung and breast cancers; intended PhaseIII first-line triple-negative breast cancer. AZ or Daiichi sponsors; parties supply drugs and share costs while retaining rights. Distinct from September28 Sone-Ve GI collaboration/equity announcement.
Full responsible original announcement inspected in web source reader; agency register inspected for original call date.
U.S. Department of Energy. Energy Department Announces Up to $400 Million for Basic Research to Advance the Frontiers of Science. DOE announcement; 2026; Official announcement. Accessed 2026-10-04T16:17:47.867Z.
Source evidence and access
Opening; seven programme offices; annual Open Call
Up to$400m FY2027 basic research, annual open solicitation covering seven Office of Science programmes including Basic Energy Sciences, advanced scientific computing, biological/environmental research, fusion/high energy/nuclear physics,isotopes. Topics without dedicated topical NOFO; application call not awards.
Full responsible original announcement inspected in web source reader; agency register inspected for original call date.
U.S. Department of Energy Office of Science. FY 2027 Continuation of Solicitation for the Office of Science Financial Assistance Program. Official funding-opportunity register; 2026; Official announcement. Accessed 2026-10-04T16:17:47.867Z.
Source evidence and access
FY2027 Continuation of Solicitation DE-FOA-0003665
DE-FOA-0003665 posted September30,2026; close September30,2027 or superseding solicitation. Applications anytime with programme-specific panels/preapplication timing. Source establishes actual original call chronology.
Full responsible original announcement inspected in web source reader; agency register inspected for original call date.
Pushmeet Kohli, David Stutz, Ali Cowen-Rivers and Jeremy Ratcliff. Introducing SynthID Bio. Google DeepMind announcement; 2026; Official announcement. Accessed 2026-10-04T16:34:51.684Z.
Source evidence and access
Looking ahead; How SynthID Bio works
September30announcement explicitly open-sources code/invitrodata and releasesweights toresearchcommunity. Family forsequence/structurewatermarking; proof-of-concept; furtherresearch/communitycollaboration andtamperrobustness needed. Newsfocus is resource availability, not repeating researchpaperresults.
Full original announcement inspected, including Looking ahead release/access statement.
Google DeepMind. SynthID Bio: Biological Sequence and Structure Watermarking. Official source-code repository; 2026; Official software resource. Accessed 2026-10-04T16:34:51.684Z.
Source evidence and access
Overview; SynthID Bio-Structure; SynthID Bio-Sequence
README providesProteinMPNNwatermarkintegration and standalonecalculator; structure branchpoints toAF3weightsinstructions. RepositoryAPIcreatedSep29,pushedSep30; initialcommitauthordate2022 is importedcommitmetadata and is notpublicrelease date. ActualpublicannouncementSeptember30 definesnewaccessdevelopment; do not claim repositorycreatedSeptember30.
RepositoryREADMEandfilelisting personallyinspected; no codeexecuted.
Publication record
Published 2026-10-04.
Sources, selection and claims were checked in an independent AI editorial review, followed by the AI editor's approval. This is not academic peer review.
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