Pharmazz Inc. and Dr. Reddy's Laboratories have entered into a licensing agreement to market Centhaquine (Lyfaquin) as a resuscitative agent for hypovolemic shock in India
22 Marzo 2024 - 12:00PM
Pharmazz, Inc. ("Pharmazz"), a biopharmaceutical company developing
and commercializing drug products to treat critically ill patients,
announced that it has entered into a license agreement with Dr.
Reddy's Laboratories Limited ("Dr. Reddy's"), a global
pharmaceutical company, to commercialize a first-in-class
innovative drug Centhaquine in India. Developed by Pharmazz for
potential global use, Centhaquine is a resuscitative agent
presently indicated for treating hypovolemic shock by Drugs
Controller General of India (DCGI).
As per the agreement, Dr. Reddy's has received
exclusive rights to market and distribute Centhaquine in India.
Pharmazz will be entitled to upfront payments and royalties. Dr.
Reddy’s will market the product under the brand name Lyfaquin®,
which it shall own. In addition to India, Dr. Reddy’s also receives
marketing rights for Lyfaquin® from Pharmazz for Nepal.
The inventor, Dr. Prof. Anil Gulati, M.D.,
Ph.D., who is the CEO and Chairman of the Board of Pharmazz, said:
"India's emergence as a hub for developing and introducing
innovative medicines is a remarkable achievement. It reflects the
country's growing capabilities in research and development within
the pharmaceutical sector. It is a large step for Pharmazz to
partner with Dr. Reddy's, a leading global pharmaceutical company
from India. For patients with hypovolemic shock, I believe Dr.
Reddy's is the best partner for Pharmazz to market Centhaquine, an
innovative, first-in-class novel resuscitative agent, in
India."
M.V. Ramana, Chief Executive Officer, Branded
Markets (India and Emerging Markets), Dr. Reddy’s, said: “The
partnership with Pharmazz and launch of this first-in-class drug
marks the latest in our effort to enter into strategic
collaborations to bring novel molecules to India to meet genuine
unmet patient needs. The clinical studies for Lyfaquin® have
demonstrated significantly better and promising outcomes, making it
as a potential add-on drug in the management of hypovolemic shock
and enhancing the current standard of care for its treatment in
India.”
Centhaquine is a frontline therapy used along
with the standard of care and is well-positioned to a critical
unmet need as a pharmacologically active resuscitative agent. A
decrease in the volume of blood circulation from blood or fluid
loss due to trauma, gastrointestinal bleeding, major surgery,
postpartum hemorrhage, diarrhea, or vomiting can cause hypovolemic
shock. About 1.9 million people worldwide die because of
hemorrhagic shock every year, most dying within the first 6 hours.
Centhaquine activates venous alpha2B adrenergic receptors to
increase cardiac preload and activates central alpha2A adrenergic
receptors to decrease cardiac afterload. Thereby, Centhaquine
converts the venous unstressed blood volume to stressed blood
volume and improves cardiac output and blood circulation, making it
an ideal candidate for the resuscitation of patients with
hypovolemic shock.
Centhaquine was approved in India by Drugs
Controller General of India following a successful Ph III clinical
trial there, the results of which are published in a manuscript
titled "A Multicentric, Randomized, Controlled Ph III Study of
Centhaquine (Lyfaquin, as a Resuscitative Agent in Hypovolemic
Shock Patients." The manuscript is published in DRUGS and is
available at:
https://link.springer.com/article/10.1007/s40265-021-01547-5.
Pharmazz received permission from the U.S. Food
and Drug Administration (FDA) to conduct a Phase III clinical trial
of Centhaquine in hypovolemic shock patients. It assesses the
safety and efficacy of Centhaquine in patients with hypovolemic
shock. The Phase III randomized double-blind, placebo-controlled
study will be conducted in 430 patients, where patients will
receive either an intravenous infusion of 0.01 mg/Kg of Centhaquine
or a placebo. All patients will receive the standard of care. A
28-day all-cause mortality is the primary endpoint.
The Phase III clinical trial is registered at
clinicaltrials.gov (NCT05251181), providing details of the trial
design and all the endpoints. U.S. FDA clearance of our Phase III
IND is an important milestone for Pharmazz and the potential future
treatment of hypovolemic shock patients.
About Pharmazz, Inc.
Pharmazz is a privately held company developing novel products in
critical care medicine. Pharmazz, Inc. obtained marketing
authorization for two of its first-in-class drug molecules,
Centhaquine and Sovateltide, for hypovolemic shock and ischemic
stroke, respectively, in India. In addition, the U.S. Food and Drug
Administration (FDA) has approved two phase III INDs for
Centhaquine as an agent for hypovolemic shock and Sovateltide for
cerebral ischemic stroke. Additional information may be found on
the Company's website, www.pharmazz.com.
Contacts: Pharmazz, Inc.
Investors David Costello |
MediaShruti Gulati |
|
Tel: |
+1 630 780 6087 |
|
Tel: |
+1 630 780 6087 |
Email: |
david.costello@pharmazz.com |
|
Email: |
shruti.gulati@pharmazz.com |
About Dr. Reddy’s: Dr. Reddy’s
Laboratories Ltd. (BSE: 500124, NSE: DRREDDY, NYSE: RDY, NSEIFSC:
DRREDDY) is a global pharmaceutical company headquartered in
Hyderabad, India. Established in 1984, we are committed to
providing access to affordable and innovative medicines. Driven by
our purpose of ‘Good Health Can’t Wait’, we offer a portfolio of
products and services including APIs, generics, branded generics,
biosimilars and OTC. Our major therapeutic areas of focus are
gastrointestinal, cardiovascular, diabetology, oncology, pain
management and dermatology. Our major markets include – USA, India,
Russia & CIS countries, China, Brazil and Europe. As a company
with a history of deep science that has led to several industry
firsts, we continue to plan ahead and invest in businesses of the
future. As an early adopter of sustainability and ESG actions, we
released our first Sustainability Report in 2004. Our current ESG
goals aim to set the bar high in environmental stewardship; access
and affordability for patients; diversity; and governance. For more
information, log on to: www.drreddys.com.
CONTACTS:
Investor RelationsRicha
PeriwalRichaperiwal@drreddys.com |
Media RelationsUsha
IyerUshaiyer@drreddys.com |
Grafico Azioni Dr Reddys Laboratories (NYSE:RDY)
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Da Dic 2024 a Gen 2025
Grafico Azioni Dr Reddys Laboratories (NYSE:RDY)
Storico
Da Gen 2024 a Gen 2025