June 5 (Reuters) - Zealand Pharma said on
Friday its experimental obesity drug, co-developed with Swiss
partner Roche, showed encouraging tolerability in a
mid-stage trial, bolstering its push to take on market leaders
with a potentially gentler alternative to existing blockbuster
treatments.
Here are some details:
* Denmark's Zealand said only 1.5% of patients who received
once-weekly subcutaneous injections of the drug, petrelintide,
discontinued treatment due to gastrointestinal side effects,
based on results presented at the American Diabetes Association
meeting in New Orleans.
* Most gastrointestinal side effects, including nausea and
vomiting, were mild.
* About 19.6% of patients experienced nausea and 3% reported
vomiting, compared with 6.2% in the placebo group. Fewer than
7.5% of patients in both groups reported diarrhea or
constipation.
* Petrelintide also improved key cardiovascular risk
factors, including reducing levels of a protein linked to
inflammation, lowering waist circumference and triglycerides, a
type of fat, more than placebo.
* Zealand had reported in March that petrelintide drove
weight loss of up to 10.7% over 42 weeks in a 493-patient study.
* Those results, however, fell short of investor
expectations, erasing billions of dollars from the company's
market value after trailing data of a rival amylin-based
candidate from Eli Lilly ( LLY ) showed up to 20.1% weight loss
in a comparable mid-stage trial.
* Zealand is seeking to break into the lucrative obesity
drug market, betting that its medicines could offer fewer and
less severe side effects than blockbuster treatments Zepbound
and Wegovy from market leaders Lilly and Novo Nordisk
.
* Unlike Wegovy and Zepbound, which target the GLP-1 hormone
to reduce appetite, amylin-based drugs such as petrelintide,
activate receptors in the brain and slow gastric emptying with
the potential for less severe side effects and preservation of
muscle.
* Roche gained access to petrelintide through an up to $5.3
billion collaboration and licensing deal last year.