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Upfront Briefing

ASH weekend delivered a firehose of hematology readouts, from bleeding disorders and sickle cell to multiple myeloma and AML. Regulators grabbed headlines too: ACIP walked back universal hep B birth dosing while FDA turmoil stoked fresh public‑health worries.

On the money side, Freenome is heading public via a $330M SPAC, Natera is bulking up in MRD, and XBI keeps grinding higher as investors lean into oncology, gene therapy, and rare neuro plays.

Tape Action

Instrument Last close 1D % YTD %
S&P 500 6,869.1 0.2% 16.8%
Nasdaq 100 25,689.5 0.4% 22.3%
Russell 2000 2,521.6 (0.4%) 13.1%
XBI 123.4 0.1% 37.0%
Nasdaq Biotech Index 5,738.8 (0.4%) 33.1%

The Big 3

1
ASH 2025 spotlights promising new data in blood disorders, cancer
  • ASH 2025 brings new clinical data on therapies for blood disorders and cancers, with updates from Star, Gilead, and others.
  • Why it matters: New clinical data from ASH 2025 highlight promising therapies for blood disorders and cancers, potentially impacting treatment standards.
  • Source: Endpoints
  • More: STAT; STAT; Fierce Biotech
2
ACIP changes hepatitis B vaccine birth dose guidance
  • ACIP has dropped its universal hepatitis B birth dose recommendation, potentially affecting vaccination protocols and public health.
  • Why it matters: ACIP's decision to drop universal hepatitis B birth dose recommendation may impact vaccination protocols and public health policies.
  • Source: Endpoints
  • More: BioPharma Dive; Fierce Pharma
3
Freenome to go public via $330M SPAC deal
  • Freenome will go public through a $330M SPAC deal, reflecting investor interest in early cancer detection and biotech IPOs.
  • Why it matters: Freenome's SPAC deal highlights ongoing investor interest in early cancer detection technologies and biotech IPO activity.
  • Source: STAT
  • More: Fierce Biotech

Everything Else that broke

  • Praxis Precision Medicines reports early efficacy success in a rare epilepsy trial, advancing clinical development for genetic epilepsies. Endpoints
  • Breyanzi's FDA approval for marginal zone lymphoma expands treatment options for rare lymphoma patients and marks a CAR-T milestone. Endpoints
  • A German court has blocked Merck's subcutaneous Keytruda launch due to a patent dispute with Halozyme, delaying market access. Endpoints
  • Five-year data confirm Hemgenix's sustained bleeding reduction, supporting gene therapy's role in hemophilia B treatment. Fierce Pharma
  • Industry voices warn that FDA instability threatens public trust and could impact drug development and approvals. Fierce Pharma

Deal Flow

M&A / BD&L

  • Natera is acquiring Foresight Diagnostics in a deal worth up to $450M, expanding its cancer testing portfolio. Fierce Biotech

VC / Private Financings

  • OTR Therapeutics has raised $100M from Pfizer Ventures and others to expand its asset portfolio and drug development. Endpoints

IPOs / Follow-Ons

  • Freenome will go public through a $330M SPAC deal, reflecting investor interest in early cancer detection and biotech IPOs. STAT

Academic Corner

  • No notable academic headlines since the last edition.
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