*
Aficamten shows cardiac benefits over blood pressure drug
metoprolol
*
Analysts see potential for aficamten to replace
beta-blocker
drugs for treating HCM
*
Cytokinetics ( CYTK ) plans to submit data to regulators for
expanded use
next year
By Bhanvi Satija and Mariam Sunny
Aug 30 (Reuters) - Cytokinetics' ( CYTK ) experimental
drug improved symptoms such as shortness of breath and chest
pain better than a standard-of-care treatment in patients with a
type of heart condition, detailed late-stage study data on
Sunday showed.
The findings, presented at the European Society of
Cardiology Congress in Madrid, Spain, augment the promising
evidence shared in May for the effectiveness of the drug,
aficamten, over current treatments.
Detailed results of the 175-patient trial indicated
aficamten had clear cardiac benefits over the blood pressure
drug metoprolol in the head-to-head study, including reduced
blockage and improved blood outflow from the heart.
The U.S. health regulator is expected to decide by December
on the drug for patients whether or not they received the
current standard treatment.
After 24 weeks, patients with obstructive hypertrophic
cardiomyopathy, an inherited condition, given aficamten showed
an average increase of 1.1 millilitre per kg/minute in peak
oxygen uptake, a key measure of heart function, while those on
metoprolol saw a decline.
Over half of the aficamten patients showed an improvement in
physical limitations, compared to 26% on metoprolol. Patients
reported improved quality of life as measured on a commonly used
questionnaire.
Some analysts have said aficamten has the potential to
replace metoprolol, which belongs to a class of drugs called
beta-blockers, as the first treatment given to patients with the
heart condition.
"This study provides profound grounds for replacing
beta-blockers by aficamten," said cardiologist and one of the
principal investigators Dr. Pablo García-Pavia.
The drug reduces the forceful heart muscle contractions
linked to the condition, Cytokinetics ( CYTK ) said. It belongs to the
same drug class as Bristol Myers Squibb's ( BMY ) approved
treatment Camzyos.
CEO Robert Blum said Cytokinetics ( CYTK ) plans to submit this data
to regulators next year for expanded use of the drug.
RBC Capital analysts have estimated $900 million in peak
sales for aficamten as a first-line treatment alone by 2034.
(Reporting by Bhanvi Satija and Mariam Sunny in Bengaluru;
Editing by Sriraj Kalluvila)