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Where capital is flowing and why the tape moves, across funding rounds, M&A, IPOs and market analysis.

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TRex Bio Targets $111.3M IPO, As Retension And Lycia Join A Busy 2026 Listing WindowOct 6, 2026

TRex Bio Targets $111.3M IPO, As Retension And Lycia Join A Busy 2026 Listing Window

TRex Bio, Retension Pharmaceuticals and Lycia Therapeutics each moved a step closer to the Nasdaq with fresh SEC filings. The filings show a market still willing to fund development-stage biotech, but also one where companies are going public with highly specific use-of-proceeds plans tied to clinical execution.

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Viking Therapeutics Closed About $575 Million After VK2735 Phase 1 Data, But Ended September Down 3.18%Oct 6, 2026

Viking Therapeutics Closed About $575 Million After VK2735 Phase 1 Data, But Ended September Down 3.18%

September trading in biotech was relatively muted at the index level, with the XBI down 3.5% for the month, but individual names still saw large swings tied to data and financing. Viking Therapeutics and Longeveron offered a clear split between a company able to raise fresh capital off positive obesity data and one forced into strategic review after its lead asset failed.

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BMO Backs Merck’s Post-Keytruda Setup, Flags Bristol Myers’ $30-Plus Billion 2028 ExposureOct 3, 2026

BMO Backs Merck’s Post-Keytruda Setup, Flags Bristol Myers’ $30-Plus Billion 2028 Exposure

Merck still faces the industry’s largest single-product replacement challenge, with Keytruda’s loss of exclusivity beginning at the end of 2028 and putting $33 billion in revenue at risk, according to BMO’s Sept. 9 report. But BMO argues Merck has already put multiple sizable assets in place, while Bristol Myers Squibb remains more dependent on riskier readouts from a smaller set of programs.

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Adecto Shuts Down After 12 Years, Citing A Risk-Averse Market For Preclinical Cancer TargetsOct 3, 2026

Adecto Shuts Down After 12 Years, Citing A Risk-Averse Market For Preclinical Cancer Targets

The Boston-based immunotherapy startup was founded by researchers from Tufts University in 2014 to build therapies and diagnostics for ADAM8-positive cancers. Its lead preclinical program, AD100, aimed to inhibit ADAM8 and reprogram both lymphoid and myeloid cells, but the company had not reported a traditional seed or venture equity round.

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Sarepta Gains New Elevidys Data In Older Duchenne Patients, As Jefferies Points To A Turnaround PathOct 2, 2026

Sarepta Gains New Elevidys Data In Older Duchenne Patients, As Jefferies Points To A Turnaround Path

The new analysis from EMBARK and ENDEAVOR compared 25 treated patients with external controls and, according to Sarepta, showed clinically meaningful effects on ambulatory motor function, time to rise from the floor, and gait speed. For investors, the update matters because it arrives after deaths linked to the viral vector behind Elevidys and another Sarepta gene therapy, a temporary U.S. shipment suspension, and a narrowed label.

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Vertex Buys Crinetics For $10 Billion, As Biopharma M&A Slows Sharply In Q3Oct 2, 2026

Vertex Buys Crinetics For $10 Billion, As Biopharma M&A Slows Sharply In Q3

Third-quarter biopharma M&A cooled materially from the prior quarter, with spending falling to just under $30 billion across 22 transactions, according to S&P Capital IQ figures cited by BioSpace. Vertex stood out in that quieter market with a Crinetics acquisition originally tallied at $10 billion by the companies, or $8.8 billion including debt and other factors by S&P Capital IQ.

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AstraZeneca Invests $2 Billion In Summit To Expand Ivonescimab ADC CombinationsSep 29, 2026

AstraZeneca Invests $2 Billion In Summit To Expand Ivonescimab ADC Combinations

The deal has three parts: AstraZeneca will buy convertible preferred stock equivalent to about 12% of Summit at a premium to Summit’s Monday closing price, jointly fund clinical trials pairing ivonescimab with sonesitatug vedotin, and set up a nonbinding framework for additional combinations. The move signals AstraZeneca sees value in using a PD-1xVEGF bispecific as a combination backbone for its ADC portfolio ahead of a global Phase 3 readout.

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Precision Neuroscience Raises $250 Million Series D, Funding Next FDA Steps For Layer 7Sep 29, 2026

Precision Neuroscience Raises $250 Million Series D, Funding Next FDA Steps For Layer 7

The company said it has now raised $430 million in total, pairing fresh capital with an FDA 510(k) approval won in March 2025 for a temporary Layer 7 cortical interface developed with Medtronic. The investment signal is that backers are still willing to fund BCI companies that can show regulatory progress, clinical access and a path to commercialization infrastructure.

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ADARx Prices $446.3 Million IPO At $17, As City Therapeutics Files For NasdaqSep 25, 2026

ADARx Prices $446.3 Million IPO At $17, As City Therapeutics Files For Nasdaq

ADARx sold 26.25 million shares at $17, above its earlier expectations, and could raise more if underwriters exercise an option for another 3.9 million shares. A concurrent $100 million private placement from AbbVie adds strategic validation as the company funds multiple siRNA programs, while City Therapeutics signals that investor appetite for RNA remains open beyond a single issuer.

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Enveda Raises $311M Series E To Push Three Programs Toward Late-Stage DevelopmentSep 23, 2026

Enveda Raises $311M Series E To Push Three Programs Toward Late-Stage Development

Enveda said the new capital will support advancement of two programs that have already generated early human data and a third asset in phase 1, while also helping move earlier candidates into the clinic. For a company built around nature-derived chemistry and AI, the round shifts the focus from platform promise to whether it can repeatedly convert early clinical signals into a development-stage business.

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Other beats

AI in Drug Discovery

Machine learning, predictive models and computational biology: how AI is changing discovery workflows and probability of success.

Biopharmaceutical Industry

Drug development, clinical trials and industry dynamics. What changes timelines, risk and competitive positioning.

Biotech Innovation

Gene therapy, CRISPR, synthetic biology and emerging platforms. Separating what is real from what is hype, and what actually translates.

Medical Technology

Digital health, diagnostics and medical devices, and the signals that matter for adoption, reimbursement and outcomes.

Regulatory & Policy

FDA actions, approvals, policy shifts and compliance: how the rules change timelines and probability.