These days, biopharma companies rarely bring just one therapy to a therapeutic area. More often, they cultivate portfolios of treatments, sometimes with overlapping indications or patient populations. This has real advantages: it signals long-term commitment to the disease area and patient community, and provides multiple options to meet the needs of different patients.
But overlap brings risk. Without a clear strategy and effective execution, two brands from the same company can end up competing with each other, leaving HCPs scratching their heads about which product to use when. The result? Confused customers, squandered promotional spend, internal tensions, and sub-optimal performance across the portfolio.
Done right, though, co-positioning delivers clarity to HCPs, payers, and patients, while optimizing performance and fortifying market leadership.
One situation we've handled frequently at ThinkGen is when a company develops a fixed-dose combination (FDC) therapy that includes a drug already marketed as a single agent.
On paper, the FDC looks like a natural upgrade, particularly with the right "dance partner." But in real clinical practice, the single agent often remains relevant, whether for HCPs who want regimen flexibility or for patients with specific clinical needs. Unless the company builds a clear narrative about which patients benefit from which product, and in what circumstances, both products risk cannibalizing each other.
Because internal bias can creep in, especially when teams feel loyal to their brand, a structured, evidence-based process guided by voice of customer insights is essential. Best practice typically involves five key steps:
Here is a case study that our team worked on directly, and that delivered tangible results in terms of the eventual dominance of our client's brands in the marketplace. At the time, their two antiretroviral (ARV) products were commercialized in the HIV marketplace:
Research revealed that each addressed different needs: newly diagnosed patients sought the convenience and reassurance of Product A, while HCPs treating patients with potential adherence challenges (or otherwise requiring a third agent besides the one included in Product A) valued the adaptability of Product B.
By positioning Product A as the “start strong” option and Product B as the “build your own regimen” choice, the company fostered clarity, credibility, and simplicity. Both products quickly found their lanes, minimizing cannibalization while maximizing patient coverage.
It’s also worth remembering that differentiation doesn’t always come solely from clinical data. Superior patient services -- such as adherence support, reimbursement navigation, or nurse helplines -- can be decisive in shaping prescribing decisions. In crowded categories, these services often tip the balance for both HCPs and patients.
The difference between success and failure in co-positioning often comes down to process.
That’s why a research-driven, systematic approach matters so much. Co-positioning isn’t about choosing one brand over another; it’s about giving each the space to thrive and ensuring patients get the right treatment at the right time.
As portfolios grow more complex -- with new formulations, next-generation mechanisms, and fixed-dose combinations -- co-positioning will only become more critical. The best strategies lean on robust research, disciplined analytics, and collaborative decision-making across functions.
With that foundation, companies can turn potential overlap into opportunity, ensuring that every brand contributes to the broader portfolio mission -- and every patient finds the treatment that fits their needs.