Terns' oral weight-loss drug shows promise in early study, shares jump
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[September 10, 2024]
By Mariam Sunny
(Reuters) -Terns Pharmaceuticals said its oral obesity drug reduced
weight by an average of 4.9% in an early-stage study, joining drugmakers
vying for a share of the lucrative weight-loss treatment market and
sending its shares up 27% on Monday.
The experimental treatment, TERN-601, is part of the second generation
of weight-loss drugs, which aim to offer a more convenient alternative
to injections, under development by companies including Pfizer and
Roche.
Market leaders Wegovy from Novo Nordisk and Zepbound from Eli Lilly are
both injectable drugs. The companies are also developing pills, the
market for which is expected to hit $150 billion by the early 2030s,
according to some analysts.
"We're very pleased with the totality of the data... seeing in
particular, no red flags," Mizuho analyst Graig Suvannavejh said about
Terns' drug.
The company's stock was trading at $9.93, and including Monday's gains,
was up more than 50% this year.
Terns said it plans to advance the drug into mid-stage trials next year.
"We have cash to cover next steps from this program," CFO Mark Vignola
said on a conference call.
Separately, Terns announced it has commenced a proposed stock offering
of $125 million of its shares. It intends to use the proceeds to fund
development of TERN-601, among other experimental treatments.
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A pharmacist counts prescription medication in a file photo.
REUTERS/Chris Wattie
TERN-601, which belongs to the GLP-1
class like Wegovy and Zepbound, met the main goals of safety and
tolerability in the study, the company said.
A 740-milligram dosage of the once-daily drug led to an average
weight loss of 4.9%, when adjusted for placebo rates, after four
weeks of treatment.
BMO Capital Markets analyst Etzer Darout said the once-daily dose is
important for the drug's competitive profile.
In July, Roche's experimental once-daily pill led to a
placebo-adjusted average weight loss of 6.1% within four weeks in
obese patients without diabetes in an early-stage study.
(Reporting by Mariam Sunny and Puyaan Singh in Bengaluru; Editing by
Shilpi Majumdar, Sriraj Kalluvila and Shinjini Ganguli)
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