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The unique playbook of Biohaven’s CEO

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Vlad Coric hasn’t always played by pharma’s rules — but that’s not to suggest the CEO of Biohaven hasn’t notched plenty of successes in the biz. Recently, in fact, Coric steered the company through a $11.6 billion acquisition by Pfizer, which picked up its blockbuster migraine med, Nurtec.

Throughout his career, Coric has eschewed some of the mainstay business strategies of the industry. And from the start, Biohaven, which launched in 2013 and grew out of Coric’s research in neuroscience, went against the grain.

‘’Everyone is leaving neuroscience. What makes you think you can survive here?’” he recalled people asking. “But our whole team has lived and breathed this, and (we) proved we can do this.”

After Nurtec won approval in 2020 and pulled in $462 million in sales in 2021 — a 600% jump over the previous year — Coric also resisted temptation to adopt a hellbent focus on growth. Although Biohaven could have ridden a revenue wave from Nurtec to help fuel an expansion into a larger commercial enterprise, that’s not what Coric wanted.

“If you’re in Big Pharma, it’s about: What kind of office do you have? How many direct reports? That’s how you know if you’re important,” he said. “That’s not how we are at Biohaven.”

While Coric acknowledged that the industry needs the “Pfizers of the world” to help drugs reach more patients, he believes Biohaven has a different role to play and should remain a smaller, more nimble and patient-driven enterprise.


“We want to do for patients with conditions like OCD and epilepsy what we did for those with migraines.”


“There is something healthy about having your feet to the fire. We want to live in this innovation space,” he explained. “It’s also a little scary. When we had Nurtec, we didn’t have to rely on financing. But this is who we are. We want to be an innovative, entrepreneurial engine.”

On Oct. 4, the company officially rebooted without Nurtec and its CGRP portfolio. Now that Biohaven is back to the brass tacks of clinical work with leading candidates for OCD and epilepsy, the question is: Can Coric and the company pull off another big win?

Primed for neuroscience

Coric grew up uniquely positioned to thrive in neuroscience drug development.

“My dad was a psychiatrist and my mom was a pharmacist,” he explained. “From a young age, I was interested in the biology of behaviors.”

Coric eventually followed in his father’s footsteps and became a psychiatrist treating a range of conditions, from OCD to bipolar disorder. He also saw that when it came to pharmaceutical treatments, there was little innovation. 

“Treatments are resistant to patients. (Patients) are not treatment resistant. We didn’t understand (these diseases) and we failed them,” he said.

He’s long been an assistant professor at Yale, where he conducted R&D through the Clinical Neuroscience Research Unit. But to learn the ropes of drug development, Coric eventually realized he’d have to make the leap from academia to industry, so he took a job at Bristol Myers Squibb where he worked in numerous therapeutic areas.

He also helped bring immuno-oncology to the front lines with treatments such as Yervoy and Opdivo. Still, with the industry buzzing over these breakthroughs, Coric couldn’t stop thinking about the unfinished work in neuroscience.

Pfizer logo

In October, Pfizer closed on its $11.6 billion acquisition of Biohaven’s CGRP franchise. 

Spencer Platt via Getty Images

 

“It gnawed at me thinking, ‘Where are these neuroscience treatments going to come from if all of these pharma companies aren’t focused on it?’” he recalled.

The upside was that with so many large pharmas fleeing neuroscience, scores of skilled scientists were on the hunt for a new job, and Coric also recognized there was a unique opportunity to bring together some of the best minds in the field. After building a “dream team” of leading CNS drug developers, Biohaven roared to life with Coric at the helm.

A ‘fast follower’ approach

Biohaven originally focused on Coric’s research at Yale into glutamate modulators and developed a drug called troriluzole, which is now in late-stage trials for OCD and spinocerebellar ataxia (SCA), a group of rare neurodegenerative diseases with no approved treatments.

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