Source: University
College London
Summary: About one
third (35 percent) of people who took a new drug for treating obesity lost more
than one-fifth of their total body weight, according to a major global study.
One third
(35%) of people who took a new drug for treating obesity lost more than
one-fifth (greater than or equal to 20%) of their total body weight, according
to a major global study involving UCL researchers.
The findings
from the large-scale international trial, published today in the New England
Journal for Medicine, are being hailed as a "gamechanger" for
improving the health of people with obesity and could play a major part in
helping the UK to reduce the impact of diseases, such as COVID-19.
The drug,
semaglutide, works by hijacking the body's own appetite regulating system in
the brain leading to reduced hunger and calorie intake.
Rachel
Batterham, Professor of Obesity, Diabetes and Endocrinology who leads the
Centre for Obesity Research at UCL and the UCLH Centre for Weight Management,
is one of the principal authors on the paper which involved almost 2,000 people
in 16 countries.
Professor
Batterham (UCL Medicine) said: "The findings of this study represent a
major breakthrough for improving the health of people with obesity. Three
quarters (75%) of people who received semaglutide 2.4mg lost more than 10% of
their body weight and more than one-third lost more than 20%. No other drug has
come close to producing this level of weight loss -- this really is a gamechanger.
For the first time, people can achieve through drugs what was only possible
through weight-loss surgery."
Professor
Batterham added: "The impact of obesity on health has been brought into
sharp focus by COVID-19 where obesity markedly increases the risk of dying from
the virus, as well as increasing the risk of many life-limiting serious
diseases including heart disease, type 2 diabetes, liver disease and certain
types of cancers. This drug could have major implications for UK health policy
for years to come."
The average
participant in the trial lost 15.3kg (nearly 3 stone); this was accompanied by
reductions in risk factors for heart disease and diabetes, such as waist
circumference, blood fats, blood sugar and blood pressure and reported
improvements in their overall quality of life.
The trial's
UK Chief Investigator, Professor John Wilding (University of Liverpool) said:
"This is a significant advance in the treatment of obesity. Semaglutide is
already approved and used clinically at a lower dose for treatment of diabetes,
so as doctors we are already familiar with its use. For me this is particularly
exciting as I was involved in very early studies of GLP1 (when I worked at the
Hammersmith Hospital in the 1990s we were the first to show in laboratory
studies that GLP1 affected appetite), so it is good to see this translated into
an effective treatment for people with obesity."
With
evidence from this trial, semaglutide has been submitted for regulatory
approval as a treatment for obesity to the National Institute of Clinical
Excellence (NICE), the European Medicines Agency (EMA) and the US Food and Drug
Administration (FDA).
About
the trial
The Phase
III 'STEP'* randomised controlled trial involved 1,961 adults who were either
overweight or had obesity (average weight 105kg/16.5 stone; body mass index
38kg/m2), and took place at 129 sites in 16 countries across Asia, Europe,
North America, and South America.
Participants
took a 2.4mg dose of semaglutide (or matching placebo) weekly via
subcutaneously (under the skin) injection; similar to the way people with
diabetes inject insulin. Overall, 94.3% of participants completed the 68-week
study, which started in autumn 2018.
Those taking
part also received individual face-to-face or phone counselling sessions from
registered dietitians every four weeks to help them adhere to the
reduced-calorie diet and increased physical activity, providing guidance,
behavioural strategies and motivation. Additionally, participants received
incentives such as kettle bells or food scales to mark progress and milestones.
In those
taking semaglutide, the average weight loss was 15.3kg (nearly three stone),
with a reduction in BMI of -5.54. The placebo group observed an average weight
loss of 2.6kg (0.4 stone) with a reduction in BMI of -0.92.
Those who
had taken semaglutide also saw reductions in risk factors for heart disease and
diabetes, such as waist circumference, blood fats, blood sugar and blood
pressure and reported improvements in their overall quality of life.
About
the drug
Semaglutide
is clinically approved to be used for patients with type 2 diabetes, though is
typically prescribed in much lower doses of 1mg.
The drug
possesses a compound structurally similar to (and mimics) the human
glucagon-like peptide-1 (GLP-1) hormone, which is released into the blood from
the gut after meals.
GLP-1
induces weight loss by reducing hunger, increasing feelings of fullness and
thereby helping people eat less and reduce their calorie intake.
While the
STEP study has been through Phase I and II trials, assessing the 2.4mg doses
for safety, in the Phase III trial some participants reported side effects from
the drug including mild-to-moderate nausea and diarrhoea that were transient
and generally resolved without permanent discontinuation from the study.
The
international trial was funded by the pharmaceutical company Novo Nordisk.