The challenge of valuing an early-stage company is one that entrepreneurs and investors face whenever the company needs money. It’s particularly difficult for companies developing products for a market that is not yet visible.
So, what to do? The GCS white paper “Early-Stage Life Science Company Valuation” profiles three approaches companies and investors use to assess what a company is worth. The first way is to calculate the value based on estimates of future profits. This approach is only as good as the revenue and expense input numbers, and the result is often more a test of plausibility and model building than a data-driven calculation of actual value.
A second approach is to base the value on that of similar companies that recently were sold or received investments. Each early-stage company is unique in its market opportunity, management team, intellectual property, and stage of development, but a set of comps that are broadly similar is a good starting point. The background information needed to understand each company and the deal that yielded the valuation is not easy to find. A few examples from proprietary databases or an investment bank’s client list consequently carry a lot of weight.
Finally, a number or range that comes from the investor’s collective experience may be a key element in an investment negotiation. For entrepreneurs, recognizing that these ranges exist and positioning one’s company to be at the high end of the range is a good strategy.
While entrepreneurs and investors often disagree over the value of an early-stage company, an experienced, successful VC told me, “One of the major factors driving the valuation for VCs is the need to make the entrepreneur feel like they got a fair deal”, and “There is a big difference between the junior VCs who seek zero-sum advantage and the experienced, successful VCs who seek positive-sum wins”.
You can download the “Early-Stage Life Science Company Valuation” white paper here.

Will ApoE Test become a Companion Diagnostic for Bexarotene?
The recent report in ScienceXpress (Feb 9) by researchers at Case Western University that a drug approved for cancer, bexarotene, cleared plaques and reversed behavioral symptoms in a mouse model of Alzheimer’s Disease (AD) raises the possibility that patients with early-stage disease might one day use this drug to delay progression and perhaps regain lost functions.
The underlying model is that amyloid beta protein, a by-product of neural activity, accumulates in the brain over time, eventually forming the plaques that are the hallmarks of AD. The laboratory of Gary Landreth, where the bexarotene study was performed, previously showed that Apolipoprotein E (ApoE) is an essential component of the pathway by which amyloid beta is cleared from the brain, and they hypothesized that increasing the amount of ApoE would lead to more rapid clearing. Bexarotene indirectly does this by affecting a signaling pathway in a way that increases the expression of the ApoE gene.
The E4 variant of ApoE is a known risk factor for Alzheimer’s and is less efficient at clearing amyloid beta. Given the challenges of screening for excess amyloid beta in the brains of non-symptomatic patients or patients with early Alzheimer’s, focusing on individuals with known risk factors like the E4 variant may be the most cost-effective approach to identifying those who might benefit most from the drug. Duke University patented the use of ApoE4 as a risk factor for AD in 1996 by (US Patent No. 5,508,167). It’s not clear (to me, anyway) how this IP will read on subsequent patents targeting ApoE4 as a companion diagnostic. Case Western University no doubt filed IP before the disclosure, and ReXceptor, the company that Gary Landreth and Paige Cramer, the study’s first author, founded will likely also focus on this question.
At this stage there are far more questions than answers, but it’s never too early to begin associating drugs with markers. Even if this therapeutic does not make the jump from mice to men, research into this novel approach will lead to discoveries and drugs that could make a real difference for the 5.4 million in the US and millions more worldwide suffering from this horrible disease.