Averitas Pharma Announces FDA Acceptance of sNDA Filing for QUTENZA® (capsaicin) 8% Patch for the Treatment of Neuropathic Pain Associated with Diabetic Peripheral Neuropathy

Morristown, N.J. (ots) - · PDUFA date set for July 19, 2020

· If approved, QUTENZA would be the first topical treatment with a TRPV1 agonist
indicated for the treatment of neuropathic pain associated with diabetic
peripheral neuropathy.

Averitas Pharma, Inc., a subsidiary of GRT US Holding, Inc. and member of the
Grünenthal Group, announced today that the supplemental New Drug Application
(sNDA) for QUTENZA for the treatment of neuropathic pain associated with
diabetic peripheral neuropathy has been accepted for review by the U.S. Food and
Drug Administration (FDA). The FDA has set a goal date under the Prescription
Drug User Fee Act (PDUFA) of July 19, 2020.

"This is a great step forward for Averitas and moves us closer towards our goal
of getting QUTENZA FDA approved for this indication," says Gabriel Baertschi,
CEO Grünenthal. "There are millions of patients with painful diabetic peripheral
neuropathy who have so far struggled to find effective pain relief. Offering
solutions for these patients' unmet needs is fully in line with our vision of
working towards a world free of pain."

About neuropathic pain associated with Diabetic Peripheral Neuropathy

Diabetes is a group of diseases marked by high levels of blood glucose resulting
from defects in insulin production, insulin action or both. According to the
American Diabetes Association, in 2015, 30.3 million Americans, or 9.4% of the
population, had diabetes.1 Diabetic neuropathies are the most prevalent chronic
complications of diabetes.2 Long-standing peripheral neuropathic pain associated
with peripheral neuropathy occurs in one of six diabetic subjects.3 Painful
diabetic neuropathy is pain arising as a direct consequence of abnormalities of
the somatosensory system in diabetic patients and predominantly affects the feet
and legs.4 People with diabetes can develop nerve problems at any time, but risk
rises with age, duration of diabetes, glucose control and presence of diabetic
retinopathy.5

About QUTENZA

QUTENZA is approved in the US for the management of neuropathic pain associated
with postherpetic neuralgia. A single, 1-hour, local topical treatment with
QUTENZA to the intact skin may provide up to 3 months of pain relief from
post-shingles nerve pain (PHN) and may be repeated every 90 days or as warranted
by the return of pain (not more frequently than every three months). QUTENZA
delivers high concentrations of the TRPV1 agonist, capsaicin through the skin,
directly to the damaged nerves that are the source of neuropathic pain. The
spontaneous activity of the TRPV1 sensitive nerves decreases and consequently
also the neuropathic pain intensity. Important safety information can be found
here: www.qutenza.com

Indication:

QUTENZA is indicated for the management of neuropathic pain associated with
postherpetic neuralgia.

IMPORTANT SAFETY INFORMATION:

Only physicians or healthcare professionals under the close supervision of a
physician are to administer QUTENZA.

Contraindications:

None

Warnings and Precautions:

-Do not apply QUTENZA to the face or scalp to avoid risk of exposure to the eyes
or mucous membranes.

-Aerosolization of capsaicin can occur and inhalation may result in coughing or
sneezing.

-If skin not intended to be treated comes into contact with QUTENZA, clean area
using Cleansing Gel.

-Patients may experience substantial procedural pain. Prepare to treat pain with
local cooling (such as a cold pack) and/or appropriate analgesic medication.

-Transient increases in blood pressure may occur during and shortly after the
QUTENZA treatment. Blood pressure changes were associated with treatment-related
increases in pain. Monitor blood pressure and provide adequate support for
treatment-related pain. Patients with unstable or poorly controlled hypertension
or a recent history of cardiovascular or cerebrovascular events may be at an
increased risk of adverse cardiovascular effects. Consider these factors prior
to initiating QUTENZA treatment.

-If opioids are used to treat pain associated with the application procedure,
please note that opioid treatment may affect the patient's ability to perform
potentially hazardous activities such as driving or operating heavy machinery.

Adverse Reactions:

In clinical trials, serious adverse reactions included application associated
pain and increase in blood pressure. The most common adverse reactions (>= 5%
and greater than control) were application-site erythema, application-site pain,
application-site pruritus, or application-site papules, and nausea.

To report an adverse event, you can visit www.fda.gov/medwatch or call
1-800-FDA-1088; or you can call Averitas Pharma, Inc. at 1-877-900-6479.

Please click here for full Prescribing Information
(https://www.qutenza.com/pdfs/Qutenza_Prescribing_Information.pdf)

About Averitas Pharma, Inc.

Averitas Pharma is a revenue-generating, specialty pharmaceutical company
dedicated to delivering innovative, effective, non-opioid pain management
options to patients in the US. The company was formed in 2018, as a subsidiary
of GRT US Holding, Inc. and member of the Grünenthal Group.

About Grünenthal

Grünenthal is a global leader in pain management and related diseases. As a
science-based, privately-owned pharmaceutical organization, we have a long track
record of bringing innovative treatments and state-of-the-art technologies to
patients worldwide. Our purpose is to change lives for the better - and
innovation is our passion. We are focussing all of our activities and efforts on
working towards our vision of a world free of pain.

Grünenthal is headquartered in Aachen, Germany, and has affiliates in 30
countries across Europe, Latin America and the US. Our products are available in
more than 100 countries. In 2018, Grünenthal employed around 4,900 people and
achieved sales of EUR 1.3 bn.

More information: www.grunenthal.com

Follow us on:

LinkedIn: Grunenthal Group
(https://www.linkedin.com/company/gruenenthal?originalSubdomain=de)

Twitter: @grunenthalgroup (https://twitter.com/grunenthalgroup?lang=de)

Instagram: grunenthal (https://www.instagram.com/grunenthal/?hl=de)

References:

1. https://www.diabetes.org/resources/statistics/statistics-about-diabetes#sthas
h.UazYaIIe.dpuf.

2. Pop-Busui R, et al.: Diabetic Neuropathy: A Position Statement by the
American Diabetes Association. Diabetes Care 2017 Jan; 40(1): 136-154

3. Daousi C, MacFarlane IA, Woodward A, Nurmikko TJ, Bundred PE, Benbow SJ:
Chronic painful peripheral neuropathy in an urban community: a controlled
comparison of people with and without diabetes. Diabet Med 2004, 21:976-982

4. Rajan R, et al: Painful diabetic neuropathy. Continuing Education in
Anaesthesia Critical Care & Pain, 2014, 14 (5): 230-235

5. Xiuxiu Liu,et al: The risk factors for diabetic peripheral neuropathy: A
meta-analysis. PLOS ONE | https://doi.org/10.1371/journal.pone.0212574 February
20, 2019

For further information, please contact:

Stepan Kracala , Head Global Communications
Tel.: +49 241 569-1335, Stepan.Kracala@grunenthal.com
Grünenthal GmbH, 52099 Aachen, Germany

Additional content: https://www.presseportal.de/pm/118252/4473028
OTS: Grünenthal Group

Original-Content von: Grünenthal Group, übermittelt durch news aktuell