Clinigen divests global rights to four cancer support therapies in support of move to solidify services.
In its continued efforts to increase the company’s focus on its pharmaceutical services market, Clinigen has divested four cancer supportive care products from its brands portfolio to CNX Therapeutics, a specialty pharmaceutical company. Those products, Cardioxane®, Savene®, Totect® and Ethyol®, address side effects patients may experience when treated with other cancer therapies. The financial terms for the divestment were not disclosed. Earlier this year, Clinigen sold Proleukin® to Iovance Biotherapeutics.
It also divested its European-based contract development business Lamda Laboratories SA, to Adragos Pharma GmbH. And late last year, Clinigen acquired Drug Safety Navigator, a specialist pharmacovigilance service provider based in the US.
The Clinigen services portfolio includes clinical trials sourcing, clinical supplies management, managed access and pharmacovigilance.
Jerome Charton, CEO of Clinigen, commented in a press release, “This divestment marks another milestone in Clinigen’s continued strategic evolution towards providing high-value services to the pharmaceutical and biotech sectors. These medicines have been integral to Clinigen, but as we refocus our efforts, it is crucial to align our offerings with our core strategy…”
Reference: “Clinigen divests global rights to four cancer support therapies to CNX Therapeutics,” 8/10/23. Clinigen press release.
Improving Relationships and Diversifying the Site Selection Process
April 17th 2025In this episode of the Applied Clinical Trials Podcast, Liz Beatty, co-founder and chief strategy officer, Inato, discusses a number of topics around site engagement including community-based sites, the role of technology in improving site/sponsor relationships, how increased operational costs are impacting the industry, and more.
Behind the Buzz: Why Clinical Research Leaders Flock to SCOPE Summit
February 7th 2025In this episode, we meet with Micah Lieberman, Executive Conference Director for SCOPE Summit (Summit for Clinical Ops Executives) at Cambridge Innovation Institute. We will dive deep into the critical role of collaboration within the clinical research ecosystem. How do we bring together diverse stakeholders—sponsors, CROs, clinical trial tech innovators, suppliers, patients, sites, advocacy organizations, investors, and non-profits—to share best practices in trial design, program planning, innovation, and clinical operations? We’ll explore why it’s vital for thought leaders to step beyond their own organizations and learn from others, exchanging ideas that drive advancements in clinical research. Additionally, we’ll discuss the pivotal role of scientific conferences like SCOPE Summit in fostering these essential connections and collaborations, helping shape the future of clinical trials. Join us as we uncover how collective wisdom and cross-industry partnerships are transforming the landscape of clinical research.
FDA-Approved Gene Therapy Beqvez Shows Sustained Efficacy, Safety in Long-Term Hemophilia B Trial
April 17th 2025Beqvez (fidanacogene elaparvovec), an FDA-approved one-time gene therapy for hemophilia B, demonstrated sustained factor IX expression, low bleeding rates, and a favorable safety profile over long-term follow-up.