Cellerant adds two new management components

Cellerant Therapeutics, a biotechnology company which specialises in therapies for blood disorders, has appointed Dr Margaret Dillon as vice president of regulatory affairs and Dr Robert Tressler as vice president of research and development. Dr Dillon comes to Cellerant with 19 years of experience in pharmaceutical regulatory affairs, most recently with CV Therapeutics (now Gilead Sciences). Dr Tressler brings to the table 20 years of industry experience in oncology, cardiovascular and immunological indications. Most recently, he served as executive director of research for Geron.

Cellerant Therapeutics, a biotechnology company which specialises in therapies for blood disorders, has appointed Dr Margaret Dillon as vice president of regulatory affairs and Dr Robert Tressler as vice president of research and development. Dr Dillon comes to Cellerant with 19 years of experience in pharmaceutical regulatory affairs, most recently with CV Therapeutics (now Gilead Sciences). Dr Tressler brings to the table 20 years of industry experience in oncology, cardiovascular and immunological indications. Most recently, he served as executive director of research for Geron.

Read the full article – start your free trial today!

Join thousands of industry professionals who rely on Scrip for daily insights

  • Start your 7-day free trial
  • Explore trusted news, analysis, and insights
  • Access comprehensive global coverage
  • Enjoy instant access – no credit card required

More from Archive

Final Chance To Have Your Say: Take Scrip's Reader Survey This Week

 

Editor’s note: This is your final call to participate in the survey to better understand our subscribers’ content and delivery needs. The deadline is 20 September.

Shape Our Content: Take The Reader Survey

 

Editor’s note: We are conducting a survey to better understand our subscribers’ content and delivery needs. If there are any changes you’d like to see in the coverage topics, content format or the method in which you receive and access Scrip, or if you love it how it is, now is the time to have your voice heard.

Galapagos Expands Point-Of-Care CAR-T Study To The US

 

CEO Paul Stoffels said gaining US clearance for an IND for its novel CAR-T product was demanding, but now opens up a pathway towards a pivotal study starting in 2025.

Analysts Split On Eisai’s Chances Of Changing EU Regulator’s Mind On Leqembi

 

A final rejection of Leqembi could also spell the same fate for Lilly’s rival drug but public outcry and demand for Alzheimer’s therapies might force the regulator’s hand

More from Scrip

Bayer Boss Cautious On Late-Stage Deals Despite Beyonttra Success

 
• By 

CEO Bill Anderson tells Scrip that the German group looks at potential in-licensing opportunities across every stage of the pipeline “but as you know, good value is a lot harder to come by in the late stage.”

Investors Shower Chinese In Vivo CAR-T Biotechs With Quick Cash

 

Byterna, Starna, Vivacta and DeliNova ride surging investor sentiment on in vivo CAR-T assets to secure venture funding.

MASH Updates: Sagimet, Altimmune, GSK Discuss Development Plans At AASLD

 
• By 

Sagimet may shift focus to later-stage MASH while it lines up Phase III financing. Altimmune expects its dual agonist to show efficacy and tolerability, while GSK is readying efimosfermin as the third FGF21 analog into Phase III for MASH.