In 2020, as a biochemistry doctoral student at UNC-Chapel Hill, Brianna Vickerman made the kind of lab breakthrough scientists dream about — a new way to control the precise location, timing and dosing of a drug using light-activated materials. Her innovation could potentially revolutionize treatment for all sorts of conditions, from life-threatening blood clots to cancer.
Though she dreamed of launching a company and creating a therapeutic platform to benefit patients, Vickerman was trained as a scientist, not an entrepreneur. She needed to learn how to commercialize her research, a process known as translational science. Enter the Eshelman Innovation Translational Academy.
The Translational Academy provides entrepreneurial education and support for innovators and early-career faculty. It’s based in the reality that turning a lab discovery into a beneficial healthcare product or service can be a long and arduous journey riddled with risk. Most startups fail — up to 90%, according to some estimates. The Translational Academy improves entrepreneurial outcomes through a mix of talent development and structured translational support in an incubator setting.
Rising to 30 Under 30
Vickerman, who made her discovery while training with UNC Eshelman School of Pharmacy Professor David Lawrence, continued her light-activated therapy research as a postdoc, but as that appointment came to an end, she faced a career crossroads. Should she form a spinout company? Drop her research altogether for an industry job offering career security? The Translational Academy gave Vickerman another option: It promoted her to a faculty position and surrounded her with translational expertise and dedicated support.
The Academy paired Vickerman with a senior leadership mentor and allowed her to recruit her own advisory board of drug development and industry experts, who counsel her on technology, commercial considerations and regulatory pathways.
For example, as Vickerman struggled to envision preclinical and clinical pathways for her pioneering technology platform, she turned to one of her advisors, the co-founder of a Research Triangle biotechnology company that develops regenerative human tissue. That company overcame a similar regulatory challenge, becoming the first to receive FDA approval for a bioengineered blood vessel. Her advisor’s advice? Sometimes there is no clearcut path. That’s what makes innovation exciting. But if you think outside the box and work with FDA expertise, you can find your solution.