BridgeBio builds war chest to take on rare disease med Vyndaqel

26 September 2023
bridgebio_large

A $250 million private financing for California’s BridgeBio Pharma (Nasdaq: BBIO) will support a possible launch of acoramidis, as well as further late-stage pipeline development.

The company has released  positive Phase III data for the small molecule, which is being developed for the rare disease transthyretin amyloid cardiomyopathy (ATTR-CM).

BridgeBio will submit for approval in the USA this year, with the goal of challenging the only currently available option, Pfizer’s (NYSE: PFE) Vyndaqel (tafamidis).

This article is accessible to registered users, to continue reading please register for free.  A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.

Login to your account

Become a subscriber

 

£820

Or £77 per month

Subscribe Now
  • Unfettered access to industry-leading news, commentary and analysis in pharma and biotech.
  • Updates from clinical trials, conferences, M&A, licensing, financing, regulation, patents & legal, executive appointments, commercial strategy and financial results.
  • Daily roundup of key events in pharma and biotech.
  • Monthly in-depth briefings on Boardroom appointments and M&A news.
  • Choose from a cost-effective annual package or a flexible monthly subscription
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed

Chairman, Sanofi Aventis UK

Companies featured in this story

More ones to watch >


Today's issue

Company Spotlight





More Features in Pharmaceutical