Where Are They Now? Start-Up Revisits Cardiac Assist Companies

The market for cardiac assist devices has, in the past, been focused on end-stage patients waiting for a heart transplant, a niche market. But now, growth is accelerating in all sectors, from acute cardiac support to the long-term support of end-stage heart failure patients. Start-Up revisits CardiacAssist, CircuLite, and MicroMed.

From time to time, START-UP revisits early-stage companies it has written about in the past to find out what went according to plan and what didn’t. We’ll see if we can draw out some lessons both from the successes and failures of companies that set out to grab an opportunity in emerging markets. This month, we revisit several companies developing cardiac assist devices, pumps to support failing hearts. The cardiac assist market breaks into several segments essentially based on whether a device is designed to support a patient for hours, days, years, or forever. In the realm of short-term support, we’ve found that the acute care market for cardiac assist devices is moving along nicely. But when it comes to the chronic, long-term support of people with heart failure, progress is like watching grass grow. In particular, left ventricular assist devices (LVADs) for end-stage heart failure patients have had prolonged development phases. One start-up founded six years ago is still at the preclinical stage, and another still doesn’t have an FDA-approved product on the market even though the company was founded 14 years ago. Thoratec Corp., the market leader in ventricular assist devices with sales in 2008 of $313 million, has a 90% share in the US LVAD market and, as the first company to gain an FDA approval of an LVAD as a destination therapy, it has singlehandedly been responsible for advancing the field, opening up a large market that was once inaccessible to LVAD manufacturers. Still, start-ups looking for venture funding don’t necessarily like to use Thoratec as a model of success. Thoratec was founded in 1976 and it didn’t receive its first LVAD approval until 1994, and it continued to operate at a loss until 2002. Over more than 30 years, more than a hundred million dollars were invested in the company, and even today, it still hasn’t been able to penetrate very far into the potential multibillion-dollar market that keeps it going.

It’s somewhat surprising, given the slow and halting progress of the one success story in the field, that more than a dozen projects have been funded by venture capital firms...

Read the full article – start your free trial today!

Join thousands of industry professionals who rely on Scrip for daily insights

  • Start your 7-day free trial
  • Explore trusted news, analysis, and insights
  • Access comprehensive global coverage
  • Enjoy instant access – no credit card required

More from Strategy

Bristol Will Pay BioNTech $1.5bn Up Front To Enter PD-L1xVEGF Space

 
• By 

BMS is guaranteeing BioNTech at least $3.5bn to share development costs and potential profits on the Phase III bispecific, to compete with Summit, Merck and Pfizer.

Sanofi Plays It Safer With Blueprint Buy After Bumpy 2025

 
• By 

But the French major is still keen on early-stage M&A.

BREAKING NEWS: Sanofi Bets $9.5bn To Bag Blueprint

 
• By 

Buy boosts the French major's immunology pipeline.

Summit’s Ivonescimab Shows Significance On PFS, But Not Overall Survival

 
• By 

In a study intended to show similar benefit in western patients, PD-1/VEGF-targeting ivonescimab met a progression-free survival endpoint, but missed on OS.

More from Business

Quick Listen: Scrip’s Five Must-Know Things

 
• By 

In this week's episode: a preview of major ASCO readouts; Roivant stays patient in deals; Lilly diversifies pain pipeline with SiteOne acquisition; Nucala gets US COPD nod; and women in Indian pharma.

Summit’s Ivonescimab Shows Significance On PFS, But Not Overall Survival

 
• By 

In a study intended to show similar benefit in western patients, PD-1/VEGF-targeting ivonescimab met a progression-free survival endpoint, but missed on OS.

Sanofi Bid For Second COPD Approval Hurt By Mixed Itepekimab Data

 
• By 

One Phase III trial hits but a second study misses by a mile.