Adocia Expands Clinical Development to Obesity with Patent Applications on Short-Acting Multihormonal Combinations Administer...
May 26 2021 - 1:30AM
Adocia (Euronext Paris: FR0011184241 – ADOC), a clinical-stage
biopharmaceutical company specialized in the development of
innovative formulations of proteins and peptides announced today
that three patent families have been filed for the treatment of
metabolic diseases including obesity, NASH (Non-Alcoholic
Steato-Hepatitis), type 2 diabetes and neurodegenerative disorders.
These patents relate to combinations of short-acting hormones
administered via pump. First preclinical results obtained in obese
mice population by a combination of glucagon-exenatide
(BioChaperone® GluExe) show a weight loss of 25% versus 15% with
exenatide alone after 14 days of treatment1. A second combination
of pramlintide and exenatide (PramExe), currently in development,
also presents promising properties. The pumps used are those
already marketed for insulin therapy, and in particular
patch-pumps, which are easy to use and suitable for this purpose.
The user can adjust the maximal tolerable dose and therefore
optimize the benefit/risk balance.
"We want to establish a new therapeutic paradigm
for chronic diseases such as obesity, allowing patients greater
control over their treatment,” explained Gérard Soula, Adocia’s
CEO. "Our vision is to empower people by helping them to regain
control of their illness, by enabling them to adjust doses in real
time with the help of modern pumps and connected devices for better
adherence to long-term treatments. This is where the future is
heading: personalized medicine and patient empowerment.”
Adocia is offering a disruptive therapeutic
approach by infusing short-acting hormones via a pump so that
patients can easily and quickly adjust the doses administered, in
contrast to the current way of thinking which is to extend the
duration of action of hormones to offer weekly injections. One of
the disadvantages of long-acting hormones is the impossibility to
interrupt the side effects - particularly gastrointestinal - which
can sometimes last several days after administration.
Pharmaco-epidemiological studies on the use of once-weekly GLP-1
hormones in type 2 diabetes reveal that 48.0% of patients stop
treatment after one year, while 73.2% stopped after two years2.
Pump-infusion opens a number of
perspectives:
- The patient can gradually increase
the dose as recommended when initiating these hormonal
treatments
- The continuous infusion allows
patients to maintain weight loss effect without concentration peaks
that could cause side effects
- The patient can stop and start the
treatment at the touch of a button; side effects decrease rapidly
due to the short-acting hormones, treatment can be resumed quickly
once these effects have subsided
- The patient has the freedom for a
“day-off”, to momentarily pause treatment for greater flexibility
on professional or personal occasions, improving quality of
life
- Algorithm development and machine
learning could also improve treatment efficacy and tolerance
“Our expertise on diabetes hormones and the
potential of insulin pumps led us to expand applications to other
chronic diseases,” comments Olivier Soula, Deputy CEO and Director
of R&D at Adocia. "Our next objective is to establish clinical
proof-of-concept with good tolerance and efficacy of PramExe
administered via pump, while being well-accepted by people
suffering from obesity."
PramExe is a fixed-ratio co-formulation of an
amylin analog (pramlintide) and a GLP-1 receptor agonist
(exenatide). Pramlintide and exenatide are two hormones marketed
for the treatment of diabetes and have already demonstrated
separately positive effects on weight loss and satiety. Adocia’s
innovation lies in combining weight loss effects of these two
compounds administered with a wearable pump. Adocia’s PramExe
combination is ready to be clinical tested in humans.
About obesity and treatments
More than 650 million people worldwide, are
obese (BMI≥30 kg/m²) according to the official classification of
the World Health Organization (WHO), which declares obesity a
chronic disease and a major public health problem since 19972.
According to the WHO, 2.8 million people die each year worldwide as
a result of being overweight or obese. Currently only 2% of
patients suffering from obesity are medicated3 and only hormonal
treatments appear as a possible alternative to bariatric
surgery.
About Adocia
Adocia is a clinical-stage biotechnology company
that specializes in the development of innovative formulations of
therapeutic proteins and peptides for the treatment of diabetes and
metabolic diseases. In the diabetes field, Adocia’s portfolio of
injectable treatments is among the largest and most differentiated
of the industry, featuring five clinical-stage products and several
pre-clinical products. The proprietary BioChaperone® technological
platform is designed to enhance the effectiveness and/or safety of
therapeutic proteins while making them easier for patients to use.
Adocia customizes BioChaperone® to each protein for a given
application.
Adocia’s clinical pipeline includes four novel
insulin formulations for prandial treatment of diabetes: two
ultra-rapid formulations of insulin analog lispro (BioChaperone®
Lispro U100 and U200), a combination of basal insulin glargine and
rapid acting insulin lispro (BioChaperone® Combo) and one
combination of a prandial insulin with amylin analog pramlintide
M1Pram. The clinical pipeline also includes an aqueous formulation
of human glucagon (BioChaperone® Glucagon) for the treatment of
hypoglycemia.
Adocia preclinical pipeline includes bi-hormonal
combinations for diabetes treatment: two combinations of rapid
acting insulin analogs and Pramlintide (BioChaperone® Lispro Pram
and BioChaperone® Aspart Pram), a combination of insulin glargine
with GLP-1 receptor agonists (BioChaperone® Glargine Liraglutide).
In addition, there are two bi-hormonal products for the treatment
of obesity: a combination of glucagon and exenatide (BioChaperone®
GluExe) and a combination of pramlintide and exenatide
(PramExe).
Adocia recently added a preclinical program to
its pipeline with a cell therapy initiative focused on development
of a hydrogel scaffold for use in people with type 1 diabetes. The
first patent application supporting this program has been
filed.
Contact Adocia
AdociaGérard SoulaCEOcontactinvestisseurs@adocia.comPh: +33 4 72
610 610www.adocia.com |
MC Services AGAdocia Press Relations Europe Raimund GabrielManaging
Partneradocia@mc-services.eu Ph: +49 89 210 228 0 |
The Ruth GroupAdocia Investor Relations USAJames
SaliernoVice-President jsalierno@theruthgroup.comPh.: +1 646 536
7035 |
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Disclaimer
This press release contains certain
forward-looking statements concerning Adocia and its business. Such
forward-looking statements are based on assumptions that Adocia
considers to be reasonable. However, there can be no assurance that
the estimates contained in such forward-looking statements will be
verified, which estimates are subject to numerous risks including
the risks set forth in the “Risk Factors” section of the Universal
Registration Document filed with the French Autorité des marchés
financiers on April 20, 2021 (a copy of which is available at
www.adocia.com) and to the development of economic conditions
financial markets and the markets in which Adocia operates. The
forward-looking statements contained in this press release are also
subject to risks not yet known to Adocia or not currently
considered material by Adocia. The occurrence of all or part of
such risks could cause actual results, financial conditions,
performance, or achievements of Adocia to be materially different
from such forward-looking statements. This press release and the
information contained herein do not constitute an offer to sell or
the solicitation of an offer to buy Adocia shares in any
jurisdiction.
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1 2019 ADA - poster presentation, 7/11/2019
2 https://www.who.int/News-Room/Fact-Sheets/Detail/Obesity-And-Overweight
3 Novo Nordisk 2020 Annual report
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