pharmadog
News
when
  • Latest
  • Archive
by source
  • All Sources
  • Sources Page
Jobs
department
  • Clinical
  • Regulatory
  • Medical Affairs
  • Commercial
  • R&D / Discovery
  • Biostatistics / Data
  • Manufacturing / CMC
  • Market Access
therapeutic area
  • Oncology
  • Immunology
  • Neuroscience
  • Cardiovascular
  • Metabolic
  • Rare Disease
  • Infectious Disease
location & type
  • Remote Only
  • US Only
  • California
  • Massachusetts
  • Internships
  • Phase 3 Roles
  • All Jobs →
Drugs
by stage
  • Marketed
  • Phase 3
  • Phase 2
  • Phase 1
  • Preclinical
browse
  • Most catalysts
  • Recently active
  • All drugs →
  • Companies
  • Patent cliff
Calendar
what
  • Trial readouts
  • PDUFA dates
  • Approvals
  • Earnings
when
  • Upcoming
  • Month grid
  • Recently passed
Sign InSubscribe
pharmadog

fetch the data · sniff the signal

Discover
  • Jobs
  • News
  • Drugs
  • Calendar
  • Companies
Hubs
  • Topics
  • Patent cliff
  • Publications
  • Readouts
Tools
  • Compare
  • Search
  • Bookmarks
Trust
  • About
  • Sources
  • Contact
Legal
  • Privacy
  • Terms
  • Pricing

© 2026 pharmadog.xyz

made by humans and a good dog

  • home
  • jobs
  • news
  • search
BioPharma Dive·May 4·1 min read
save

Latus Bio raises $97 million to advance gene therapies for Huntington’s and Batten disease

May 4, 2026·read at BioPharma Dive ↗DealPositive

Latus Bio announced closing a $97 million Series A round, including a $43 million extension to a prior $54 million raise. Funding was led by 8VC and included eight other investors such as DCVC Bio and BioAdvance.

The capital will fund development of two gene‑therapy candidates moving toward clinical testing. LTS‑101 targets the CLN2 form of Batten disease, a childhood neurodegenerative disorder, and is slated to start a human trial in the third quarter of 2026.

LTS‑201 is aimed at Huntington’s disease, a progressive brain‑wasting condition that has been difficult for drug developers. Latus plans to request permission from U.S. regulators later this year to begin an early‑stage study.

The company’s approach focuses on novel viral capsids designed to deliver therapy at lower doses, a strategy that could broaden gene‑therapy applications beyond ultra‑rare diseases.

source

This writeup was produced by pharmadog from original reporting by BioPharma Dive.

Original headline: “With $97M, Latus pursues a different kind of Huntington’s gene therapy”

read at BioPharma Dive ↗
550 words · retrieved May 4
sharex / twitterlinkedin

comments(0)

5-min edit window · permanent after that
sign in to leave a comment · permanent archive after 5 minutes
no comments yet — first sniff?

companies & drugs in this story

companies
Ultragenyx Pharmaceutical Inc.4
drugs
Rare Disease
topics
Gene Therapy (AAV)7Rare Disease4Neurology2ApprovalCardiologyNephrologyOphthalmology

related stories

  • Jun 2910 clinical trials to watch in the second half of 2026BioPharma Dive
  • 4d agoGSK laying off 1.2K+ in BelgiumBioSpace
  • Dec 23Fierce Biotech Layoff Tracker 2026: Enlivex excises 60%; Eyepoint halves headcountFierce Biotech
  • Dec 22Fierce Biotech Fundraising Tracker '26: Nouscom nabs $135M series D; Estuary channels $93M series AFierce Biotech
  • Sep 23Ionis-Otsuka offer 'groundbreaking' improvement in function and survival for genetic type of ALSBioSpace