Knight Therapeutics Announces Health Canada Approval for JORNAY PM™ to Treat Attention-Deficit Hyperactivity Disorder (ADHD)
November 14 2024 - 3:30PM
Knight Therapeutics Inc. (TSX: GUD) ("Knight"), a pan-American
(ex-USA) specialty pharmaceutical company, announced today that
Health Canada has approved
JORNAY PM™, an
extended-release formulation of methylphenidate, a stimulant
medication for the treatment of Attention-Deficit Hyperactivity
Disorder (ADHD) in children.
JORNAY PM™ is the first and
only evening-dosed methylphenidate product commercially available
in Canada to treat ADHD in patients from 6 to 12 years of age.
JORNAY PM™ consists of microbeads with a
delayed-release layer and an extended-release layer. The first
layer delays the release of the active ingredient until morning
while the extended-release layer controls the release of the active
ingredient starting in the morning and continuing throughout the
day. This unique formulation provides a pharmacokinetic profile
that allows ADHD symptom control from the time patients wake up
until the evening.
“As a psychiatrist who treats ADHD, I find the
introduction of JORNAY PM™ particularly exciting
because its distinct mechanism of delivery addresses one of the
most difficult aspects of ADHD management—early morning
functioning. JORNAY PM™ offers an effective
treatment that assists in better morning routines. This new
treatment is a welcome addition to the growing options available
for ADHD management in Canada”, said Dr. Doron Almagor (MD, FRCPC)
Child, Adolescent, and Adult Psychiatrist.
JORNAY PM™ was studied in two
multicenter, randomized, double-blind, placebo-controlled, phase 3
clinical trials1,2. Both studies met their primary and key
secondary endpoints demonstrating a statistically significant and
clinically meaningful improvement in ADHD symptom control upon
awakening, through the afternoon, and into the early
evening.
“I am proud to announce the approval of
JORNAY PM™ in Canada. This exciting new launch,
expected in the second half of 2025, represents a significant
advancement for our Canadian business as we continue to expand our
offerings for ADHD treatment,” said Samira Sakhia, President and
CEO of Knight. “Following this approval, we are building a
well-rounded ADHD portfolio with a range of complementary therapies
that address diverse patient needs and offer greater support for
their families.”
In May 2024, Knight entered into an agreement
with Ironshore Pharmaceuticals & Development, Inc., a wholly
owned subsidiary of Ironshore Therapeutics, Inc. (now part of
Collegium Pharmaceutical, Inc.; Nasdaq: COLL), for the exclusive
rights to distribute JORNAY PM™ in Canada and
Latin America.
According to IQVIA Canada, the total Canadian
market of extended-release methylphenidate products was $469
million in 2023, with an 8.1% increase in prescriptions compared to
2022 and a 16% compound annual growth rate (CAGR) over the past
four years.
About
ADHD3
ADHD is a chronic, often lifelong
neurodevelopmental disorder that affects both children and adults.
The estimated prevalence of ADHD is 5-9% in children and
adolescents and 3-5% in adults. 3 The disorder is
characterized by symptoms of inattention, hyperactivity, and
impulsivity that can significantly impact an individual's
ability to function in daily life. Although patients’ symptoms of
ADHD can change over time, they will generally require continued
monitoring and treatment over their lifetime. Current first-line
pharmacotherapies for ADHD include long-acting methylphenidate or
amphetamine-based psychostimulants and non-stimulants. Individual
products for both differ in their delivery systems and release
profiles to provide distinct durations of effect. However, not all
patients derive adequate symptom coverage with currently available
therapies. As a result, there remains a significant medical need
for additional treatment options for patients with ADHD.
About Knight Therapeutics
Inc.
Knight Therapeutics Inc., headquartered in
Montreal, Canada, is a specialty pharmaceutical company focused on
acquiring or in-licensing and commercializing pharmaceutical
products for Canada and Latin America. Knight’s Latin American
subsidiaries operate under United Medical, Biotoscana Farma and
Laboratorio LKM. Knight Therapeutics Inc.'s shares trade on TSX
under the symbol GUD. For more information about Knight
Therapeutics Inc., please visit the company's web site at
www.knighttx.com or www.sedarplus.ca.
Forward-Looking Statements for
Knight
This document contains forward-looking
statements for Knight Therapeutics Inc. and its subsidiaries. These
forward-looking statements, by their nature, necessarily involve
risks and uncertainties that could cause actual results to differ
materially from those contemplated by the forward-looking
statements. Knight Therapeutics Inc. considers the assumptions on
which these forward-looking statements are based to be reasonable
at the time they were prepared but cautions the reader that these
assumptions regarding future events, many of which are beyond the
control of Knight Therapeutics Inc. and its subsidiaries, may
ultimately prove to be incorrect. Factors and risks which could
cause actual results to differ materially from current expectations
are discussed in Knight Therapeutics Inc.'s Annual Report and in
Knight Therapeutics Inc.'s Annual Information Form for the year
ended December 31, 2023, as filed on www.sedarplus.ca. Knight
Therapeutics Inc. disclaims any intention or obligation to update
or revise any forward-looking statements, whether as a result of
new information or future events, except as required by law.
References:
- Childress, A.
C., Cutler, A. J., Marraffino, A., McDonnell, M. A., Turnbow, J.
M., Brams, M., DeSousa, N. J., Incledon, B., Sallee, F. R., &
Wigal, S. B. (2020). A randomized, double-blind, placebo-controlled
study of HLD200, a delayed-release and extended-release
methylphenidate, in children with attention-deficit/hyperactivity
disorder: An evaluation of safety and efficacy throughout the day
and across settings. Journal of Child and Adolescent
Psychopharmacology, 30(1), 2–14.
https://doi.org/10.1089/cap.2019.0070
- Pliszka, S. R.,
Wilens, T. E., Bostrom, S., Arnold, V. K., Marraffino, A., Cutler,
A. J., López, F. A., DeSousa, N. J., Sallee, F. R., Incledon, B.,
& Newcorn, J. H. (2017). Efficacy and safety of HLD200,
delayed-release and extended-release methylphenidate, in children
with attention-deficit/hyperactivity disorder. Journal of Child and
Adolescent Psychopharmacology, 27(6), 474–482.
https://doi.org/10.1089/cap.2017.0084
- CADDRA -
Canadian ADHD Resource Alliance. (2020). Canadian ADHD Practice
Guidelines, 4.1 Edition.
https://adhdlearn.caddra.ca/wp-content/uploads/2022/08/Canadian-ADHD-Practice-Guidelines-4.1-January-6-2021.pdf
CONTACT INFORMATION FOR KNIGHT:
Investor Contact: |
|
Knight Therapeutics Inc. |
|
Samira Sakhia |
Arvind Utchanah |
President & Chief Executive
Officer |
Chief Financial Officer |
T: 514.484.4483 |
T. +598.2626.2344 |
F: 514.481.4116 |
|
Email: IR@knighttx.com |
Email: IR@knighttx.com |
Website: www.knighttx.com |
Website: www.knighttx.com |
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