Founders
Andrew J. Stewart Coats

Andrew J. Stewart Coats, Founder and Non-Executive Director

Professor Andrew Coats MBA, DSc, DM, co-founded Actimed Therapeutics in 2017, having  previously founded Myotec (later renamed PsiOxus Therapeutics). Andrew has over 30 years of experience as an academic manager, having been both Dean of Medicine and Deputy Vice-Chancellor at the University of Sydney and head of Clinical Cardiology at Imperial College and the Royal Brompton Hospital in London. Andrew also served as CEO of the Norwich Research Park in the UK. Andrew is an experienced board director and chairman with an MBA from London Business School. He has over 20 years of experience of company boards in roles including audit, remuneration, nominations and governance committees in biotechnology, publishing health care and education, including the George Institute of International Health, the Woolcock Institute, Lone Star Heart, Myotec, PsiOxus, Radcliffe Group, ESN Cleer and Faraday (Australia). Andrew has been on the board of the Heart Failure Association (HFA) of the ESC since 2012 and will be its President from 2020 to 2022.  He has been a member of over 20 international clinical trial steering committees in the fields of heart failure and cachexia and has over 700 career research papers, 95,000 citations and an h-Index of 130.

Stefan D. Anker

Stefan D. Anker, Founder, Non-executive Director & Chair of Scientific Advisory Board

Professor Stefan Anker MD, PhD, co-founded Actimed Therapeutics in 2017, having previously founded Myotec (later renamed PsiOxus Therapeutics). Stefan has 30 years academic research experience in heart failure, cachexia and clinical trials with positions at Royal Brompton Hospital and Imperial College in London as well as University Göttingen and Charité Berlin. Stefan has been a tenured University-Professor in Germany since 2007, leading a highly active research group, and he is founding Editor-in-Chief of two successful scientific journals (including the Journal of Cachexia, Sarcopenia and Muscle).  Stefan was Vice President of the European Society of Cardiology (ESC) from 2016 to 2018, and served on the ESC board from 2012 to 2018. He has served on the board of the Heart Failure Association (HFA) of the ESC since 2006; and was HFA President from 2012 to 2014.

Yann Colardelle

Yann Colardelle, Founder

Yann Colardelle is a professional in communications and medical education who has been involved in research and education in cachexia for more than 15 years. In 1998 he founded Medical Education Global Solutions, a leading independent medical education company with a focus on global and multidisciplinary projects.

Yann holds a degree from the University of Provence and an eMBA at Paris Dauphine.  As a founder, he envisions Actimed therapeutics as the organisation that will change the paradigm of cachexia management and improve the lives of patients and their families and carers.

Dec 13, 2024
Actimed Therapeutics Announces Publication of Successful S-pindolol benzoate (ACM-001.1) Phase 1 Study in The Journal of Cachexia, Sarcopenia and Muscle

London, UK – 13th December 2024. Actimed Therapeutics Ltd (“Actimed”), a UK based clinical stage speciality pharmaceutical company focused on bringing innovation to the treatment of cancer cachexia and other muscle wasting disorders, announces that results from its Phase 1 pharmacokinetic (PK), pharmacodynamic (PD) and bioavailability study of S-pindolol benzoate (ACM-001.1) in healthy volunteers (NCT06028321) have been published in The Journal of Cachexia, Sarcopenia and Muscle.

This was a two-stage Phase I study. The first stage assessed the comparative bioavailability and pharmacokinetics of a single dose of S-pindolol benzoate and two single doses of racemic pindolol. The second stage evaluated the steady-state pharmacokinetics and pharmacodynamics of multiple doses of S-pindolol benzoate in healthy volunteers.

The study met all pre-defined endpoints, demonstrating that S-pindolol benzoate has predictable pharmacokinetics up to a dose of 15 mg twice daily, with low inter-subject variability after single and multiple doses. Moreover, bioavailability of S-pindolol after equivalent doses of racemic pindolol and S-pindolol benzoate was comparable, and although not a prespecified objective, formal bioequivalence margins were met. 

The study also showed:

  • An absence of in vivo stereo-conversion of S-pindolol into R-pindolol
  • Dose linearity and dose proportionality of S-pindolol benzoate over a wide range of doses 
  • S-pindolol benzoate was generally well tolerated
  • A lack of food effect with S-pindolol benzoate - and an important consideration for use in cancer patients who have a high incidence of appetite loss


Robin Bhattacherjee, Chief Executive Officer of Actimed Therapeutics commented
“The anti-catabolic and pro-anabolic pharmacology of our lead compound S-pindolol benzoate position it as a novel and promising new therapy for cancer cachexia. These data demonstrate that S-pindolol benzoate is essentially bioequivalent to the S-pindolol present in racemic pindolol and provide strong support for the further clinical development of S-pindolol benzoate for the treatment of cancer cachexia and potentially other conditions associated with muscle wasting”. 

The publication may be accessed here: https://doi.org/10.1002/jcsm.13651

 

About Actimed Therapeutics  

Actimed Therapeutics is a clinical stage speciality pharmaceutical company focused on bringing innovation to the treatment of muscle wasting disorders to transform the care of an underserved and vulnerable patient population. 

The lead area of focus for Actimed is specifically in cachexia. Cachexia is a wasting disease that is associated with cancer and other serious chronic illnesses and with significant morbidity and mortality. A significant number of cancer patients suffer from cachexia1 and it is estimated that cachexia is responsible for up to 20% of all cancer deaths2. A recent meta-analysis demonstrated that cachexia was associated with an 82% higher relative risk of mortality in patients with NSCLC versus no cachexia3.

Despite its prevalence and devastating clinical effects, there is no globally approved drug for the treatment or prevention of cancer-related cachexia.  

The lead product of Actimed, S-pindolol benzoate (ACM-001.1) targets multiple pathways that drive cachexia and has generated promising proof of concept Phase 2a clinical data in cachexia patients. Actimed is currently preparing for further clinical studies in cancer cachexia having received an Investigational New Drug (IND) approval from FDA for S-pindolol benzoate in August 2023 for the treatment of cancer cachexia. 

Actimed also owns the global rights to its second asset, S-oxprenolol ACM-002), which is being developed by the Company for the muscle wasting seen in amyotrophic lateral sclerosis (ALS) where loss of body mass and muscle wasting may impact survival⁴. Actimed was granted Orphan Drug Designation to S-oxprenolol for the treatment of ALS by the FDA in 2024. Actimed has licensed the global rights to develop and commercialise S-oxprenolol 

 

 

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Frazer Hall, Erica Hollingsworth
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Email: actimed@medistrava.com