RICHMOND, Va. and SLOUGH, England, Nov.
30, 2017 /PRNewswire/ -- Indivior PLC (LON: INDV) today
announced that the U.S. Food and Drug Administration (FDA) has
approved SUBLOCADETM (buprenorphine extended- release)
injection for subcutaneous use (CIII), the first and only
once-monthly injectable buprenorphine formulation for the treatment
of moderate to severe opioid use disorder (OUD) in patients who
have initiated treatment with a transmucosal
buprenorphine-containing product followed by dose adjustment for a
minimum of seven days. SUBLOCADE is intended to be administered
only by healthcare providers and should be used as part of a
complete treatment program that includes counseling and
psychosocial support1. SUBLOCADE is expected to be
available to patients in the U.S. in Q1 2018.
Experience the interactive Multichannel News Release here:
https://www.multivu.com/players/English/8221151-indivior-sublocade-buprenorphine-fda-approval/
"SUBLOCADE is a scientific innovation that represents a new
treatment option to help patients attain more illicit opioid-free
weeks during their treatment program," said Shaun Thaxter, Chief Executive Officer of
Indivior. "In the Opioid Blockade Study, SUBLOCADE achieved
complete blockade of drug-liking effects for a full month in most
patients. SUBLOCADE is the first and only therapy that, at steady
state, delivers buprenorphine at a sustained rate of at least 2
ng/mL over a one month period. The urgency for this new treatment
has never been greater, as the U.S. opioid crisis has been declared
a national public health emergency. SUBLOCADE's approval is an
important step forward for patients, families and communities
battling the opioid epidemic."
SUBLOCADE contains buprenorphine, a partial agonist at the
mu-opioid receptor1. Mu-opioid receptors in the brain
are known to mediate the subjective effects of opioids, including
drug-liking, which is the pleasure associated with opioid
use2. SUBLOCADE delivers sustained plasma levels of
buprenorphine that translate into high mu-opioid receptor occupancy
in the brain, which blocks the drug-liking effects of
opioids1.
In the SUBLOCADE clinical trial program, average buprenorphine
plasma concentrations of 2-3 ng/mL were associated with mu-opioid
receptor occupancy ≥70% and the reduction of illicit opioid
use. SUBLOCADE 300 mg delivers average buprenorphine plasma
levels of approximately 2 ng/mL after the first injection. The
average concentration of SUBLOCADE at steady-state was 3.21 ng/mL
and 6.54 ng/mL for the 100 mg and 300 mg doses,
respectively1.
Indivior conducted an Opioid Blockade Study (RB-US-13-0002)
which investigated the ability of SUBLOCADE 300 mg to block the
subjective effects of illicit opioids, including drug-liking. In
the 12-week trial evaluating the blocking effect, SUBLOCADE 300 mg
fully blocked the drug-liking effects of
hydromorphone1. Hydromorphone is a potent opioid
pain medication3 that is commonly used in human studies
to evaluate opioid drug-liking2.
SUBLOCADE was evaluated in a 24-week, Phase 3 pivotal study
(RB-US-13-0001) in which patients were randomized to one of the
following three regimens: six once-monthly SUBLOCADE 300 mg doses;
two once-monthly SUBLOCADE 300 mg doses followed by four
once-monthly 100 mg doses; or six once-monthly injections of
placebo. Both dosage regimens of SUBLOCADE were shown to be
superior to placebo in achieving more illicit opioid-free weeks
(p<0.0001)1,4. In the clinical trials, the overall
safety profile for SUBLOCADE, given by a healthcare provider, was
consistent with the known safety profile of transmucosal
buprenorphine, except for injection site reactions. The most common
adverse reactions (≥5% patients), included constipation, nausea,
vomiting, abnormal liver enzymes, headache, sedation and
somnolence. Injection site reactions were reported in 16.5% of the
patients. None of the injection site reactions were serious,
and only one led to study treatment
discontinuation1.
"Every patient's journey to recovery is different and they face
many challenges. To help support these differences, doctors and
patients need options for medication-assisted treatment," said Dr.
Brent Boyett, SUBLOCADE clinical
investigator and director at Boyett Health Services, Inc. "In a
Phase 3 clinical study, SUBLOCADE helped patients refrain from
illicit opioids for more weeks compared to placebo. Used in
combination with counseling and psychosocial support, SUBLOCADE is
a transformational new drug that offers a treatment option for
people with moderate to severe opioid use disorder."
The opioid addiction epidemic in the U.S. is a national public
health emergency, with nearly 12 million people impacted nationwide
and an average of four people dying from opioid overdose every hour
of every day5,6,7. OUD, commonly referred to as opioid
addiction8, is a chronic disease that changes the
brain9. The patient journey to treatment and recovery is
complex, with many barriers such as social stigma, access to
treatment and prescribers, and difficulty adhering to treatment
plans. Out of the more than 2.5 million patients diagnosed with OUD
in the U.S., less than half are treated with medication-assisted
treatment (MAT)10.
The economic impact of the opioid epidemic to the healthcare
system is significant. The amount paid for treatment of substance
use disorders is only a small portion of the costs these disorders
impose on society. Data published in 2016 presented the total costs
of prescription opioid use disorder and overdose in the U.S. at
$78 billion in 2013. Of that, only
3.6 percent, or about $2.8 billion,
was for treatment11. A separate, recent analysis
by the White House Council of Economic Advisers estimated the total
annual cost of prescription opioid overdose, abuse and dependence
in the U.S. at $504 billion in the
year 201512. Patients, physicians, policymakers and
other stakeholders have expressed the need for additional treatment
options in the fight against the chronic relapsing disease of
opioid addiction. Indivior has an ongoing, prospective,
observational study (RECOVERTM) to understand the
clinical, environmental and socioeconomic characteristics of OUD
patients13.
"The American Society of Addiction Medicine supports the
development and manufacturing of medications that aid in the
treatment of addiction," said Dr. Kelly
Clark, President, American Society of Addiction Medicine.
"The introduction of novel pharmacotherapies supports this goal.
Addiction patients, like all patients, should have available to
them a robust and varied array of treatment options, as no one
treatment modality is appropriate or therapeutic for everyone."
"We applaud the scientists and leaders who have been working
tirelessly on the development of new, longer-acting medicines for
the treatment of opioid use disorder. These exciting new
developments will help our patients and families live healthy lives
and accelerate the progress in the treatment of addiction,"
commented Jessica Hulsey Nickel,
President and CEO of the Addiction Policy
Forum.
Under the Drug Addiction Treatment Act (DATA) codified at 21
U.S.C. 823(g), prescription use of SUBLOCADE in the treatment of
opioid dependence is limited to healthcare providers who meet
certain qualifying requirements, and who have notified the
Secretary of Health and Human Services (HHS) of their intent to
prescribe this product for the treatment of opioid dependence and
have been assigned a unique identification number that must be
included on every prescription1.
SUBLOCADE will be distributed through a restricted distribution
system, which is intended to prevent the direct distribution to a
patient. This is because of risk of serious harm or death that
could result from intravenous self-administration.
Indivior worked closely with the FDA to include appropriate
warnings and precautions, including a BOXED WARNING in the label
and implementation of a Risk Evaluation and Mitigation Strategy
(REMS) program. Healthcare settings and pharmacies that order and
dispense SUBLOCADE must be certified in the SUBLOCADE REMS Program.
In addition, Indivior continues to enhance its compliance program
to keep pace with the anticipated increase in the number of
patients in treatment.
About SUBLOCADE TM
INDICATION AND USAGE
SUBLOCADE is indicated for the
treatment of moderate to severe opioid use disorder in patients who
have initiated treatment with a transmucosal
buprenorphine-containing product followed by a dose adjustment
period for a minimum of seven days.
SUBLOCADE should be used as part of a complete treatment program
that includes counseling and psychosocial support.
WARNING: RISK OF
SERIOUS HARM OR DEATH WITH INTRAVENOUS ADMINISTRATION; SUBLOCADE
RISK EVALUATION AND MITIGATION STRATEGY
|
|
- Serious harm or death could result if
administered intravenously. SUBLOCADE forms a solid mass upon
contact with body fluids and may cause occlusion, local tissue
damage, and thrombo-embolic events, including life threatening
pulmonary emboli, if administered intravenously.
- Because of the risk of serious harm or
death that could result from intravenous self-administration,
SUBLOCADE is only available through a restricted program called the
SUBLOCADE REMS Program. Healthcare settings and pharmacies that
order and dispense SUBLOCADE must be certified in this program and
comply with the REMS requirements.
|
IMPORTANT SAFETY INFORMATION
Prescription use of this
product is limited under the Drug Addiction Treatment Act.
CONTRAINDICATIONS
SUBLOCADE should not be administered
to patients who have been shown to be hypersensitive to
buprenorphine or any component of the ATRIGEL® delivery system
WARNINGS AND PRECAUTIONS
Addiction, Abuse, and Misuse: SUBLOCADE
contains buprenorphine, a Schedule III controlled substance that
can be abused in a manner similar to other opioids. Monitor
patients for conditions indicative of diversion or progression of
opioid dependence and addictive behaviors.
Respiratory Depression: Life threatening
respiratory depression and death have occurred in association with
buprenorphine. Warn patients of the potential danger of
self-administration of benzodiazepines or other CNS depressants
while under treatment with SUBLOCADE.
Neonatal Opioid Withdrawal Syndrome: Neonatal opioid withdrawal
syndrome is an expected and treatable outcome of prolonged use of
opioids during pregnancy.
Adrenal Insufficiency: If diagnosed, treat with physiologic
replacement of corticosteroids, and wean patient off of the
opioid.
Risk of Opioid Withdrawal With Abrupt Discontinuation: If
treatment with SUBLOCADE is discontinued, monitor patients for
several months for withdrawal and treat appropriately.
Risk of Hepatitis, Hepatic Events: Monitor liver function tests
prior to and during treatment.
Risk of Withdrawal in Patients Dependent on Full Agonist
Opioids: Verify that patient is clinically stable on
transmucosal buprenorphine before injecting SUBLOCADE.
Treatment of Emergent Acute Pain: Treat pain with a non-opioid
analgesic whenever possible. If opioid therapy is required, monitor
patients closely because higher doses may be required for analgesic
effect.
ADVERSE REACTIONS
Adverse reactions commonly
associated with SUBLOCADE (in ≥5% of subjects) were constipation,
headache, nausea, injection site pruritus, vomiting, increased
hepatic enzymes, fatigue, and injection site pain.
The full prescribing information, including BOXED WARNING, for
SUBLOCADE can be found here:
http://indivior.com/wp-content/uploads/2017/11/SUBLOCADE-Prescribing-Information.pdf.
About Opioid Use Disorder
OUD, commonly referred to as opioid addiction8,
is a chronic, relapsing disease that changes the brain9.
According to the DSM–5, opioid use disorder is characterized by
signs and symptoms that reflect compulsive, prolonged
self-administration of opioid substances that are used for no
legitimate medical purpose or, if another medical condition is
present that requires opioid treatment, they are used in doses
greatly in excess of the amount needed for that medical
condition13.
Based on 2016 data from the most recent National Survey on Drug
Use and Health report, nearly 12 million Americans (age 12+
years) engaged in misuse of opioids in the last year6.
Between 1999 and 2014 the rate of deadly opioid overdoses
quadrupled14, and in the
United States alone, an average of four people die of opioid
overdose every hour of every day7. In 2015 opioids
accounted for 70 percent of the negative health impact associated
with drug use disorders worldwide15. Approximately 2.5
million American adults (age 18+ years old) met criteria for opioid
use disorder in the past year10. The same report
suggested that 935,000 adults have used heroin in the past year and
471,000 used in the past month. There were approximately 625,000
adults who had a heroin use disorder in the past year6.
In a recent report by the White House Council of Economic Advisers,
estimated economic costs of the opioid crisis in the U.S. were
$504 billion in
201512.
About Indivior
Indivior is a global specialty pharmaceutical company with
a 20-year legacy of leadership in patient advocacy and health
policy while providing education on evidence-based treatment models
that have revolutionized modern addiction treatment. The name is
the fusion of the words individual and endeavour, and the tagline
"Focus on you" makes the Company's commitment clear. Indivior is
dedicated to transforming addiction from a global human crisis to a
recognized and treated chronic disease. Building on its global
portfolio of opioid dependence treatments, Indivior has a strong
pipeline of product candidates designed to both expand on its
heritage in this category and address other chronic conditions and
co-occurring disorders of addiction, including alcohol use disorder
and schizophrenia. Headquartered in the
United States in Richmond,
VA, Indivior employs more than 900 individuals globally and
its portfolio of products is available in over 40 countries
worldwide. Visit www.indivior.com to learn more.
Forward-Looking Statements
This press release contains certain statements that are
forward-looking and which should be considered, amongst other
statutory provisions, in light of the safe harbour provisions of
the United States Private Securities Litigation Reform Act of 1995.
By their nature, forward-looking statements involve risk and
uncertainty as they relate to events or circumstances that will or
may occur in the future. Actual results may differ materially from
those expressed or implied in such statements because they relate
to future events. Forward-looking statements include, among other
things, statements regarding our financial guidance for 2017 and
our medium- and long-term growth outlook, our operational goals,
our product development pipeline and statements regarding ongoing
litigation.
Various factors may cause differences between Indivior's
expectations and actual results, including: factors affecting sales
of Indivior Group's products; the outcome of research and
development activities; decisions by regulatory authorities
regarding the Indivior Group's drug applications; the speed with
which regulatory authorizations, pricing approvals and product
launches may be achieved; the outcome of post-approval clinical
trials; competitive developments; difficulties or delays in
manufacturing; the impact of existing and future legislation and
regulatory provisions on product exclusivity; trends toward managed
care and healthcare cost containment; legislation or regulatory
action affecting pharmaceutical product pricing, reimbursement or
access; claims and concerns that may arise regarding the safety or
efficacy of the Indivior Group's products and product candidates;
risks related to legal proceedings; the Indivior Group's ability to
protect its patents and other intellectual property; the outcome of
patent infringement litigation relating to Indivior Group's
products, including the ongoing ANDA lawsuits; changes in
governmental laws and regulations; issues related to the
outsourcing of certain operational and staff functions to third
parties; uncertainties related to general economic, political,
business, industry, regulatory and market conditions; and the
impact of acquisitions, divestitures, restructurings, internal
reorganizations, product recalls and withdrawals and other unusual
items.
This press release does not constitute an offer to sell,
or the solicitation of an offer to subscribe for or otherwise
acquire or dispose of shares in the Company to any person in any
jurisdiction to whom it is unlawful to make such offer or
solicitation.
References
1. SUBLOCADETM (buprenorphine extended release)
label.
2. Nasser AF et al. (2016). Sustained-Release
Buprenorphine (RBP-6000) Blocks the Effects of Opioid Challenge
with Hydromorphone in Subjects with Opioid Use Disorder. J Clin
Psychopharmacol. 36(1):18-26.
3. National Institutes of Health, MedlinePlus.
Hydromorphone. Retrieved from:
https://medlineplus.gov/druginfo/meds/a682013.html. Accessed
November 29, 2017.
4. Indivior Data on File.
5. The White House Office of the Press Secretary.
(October 26, 2017). President
Donald Trump is Taking Action on
Drug Addiction and the Opioid Crisis. Retrieved from
https://www.whitehouse.gov/the-press-office/2017/10/26/president-donald-j-trump-taking-action-drug-addiction-and-opioid-crisis.
Accessed October 30, 2017.
6. Substance Abuse and Mental Health Services
Administration. (2017). Key substance use and mental health
indicators in the United States:
Results from the 2016 National Survey on Drug Use and Health (HHS
Publication No. SMA 17-5044, NSDUH Series H-52). Rockville, MD: Center for Behavioral Health
Statistics and Quality, Substance Abuse and Mental Health Services
Administration. Retrieved from
https://www.samhsa.gov/data/sites/default/files/NSDUH-FFR1-2016/NSDUH-FFR1-2016.htm.
Accessed September 11,
2017.
7. Centers for Disease Control and Prevention.
Understanding the Epidemic. Retrieved from
https://www.cdc.gov/drugoverdose/epidemic/index.html. Accessed
October 28, 2017.
8. Murthy, VH. Ending the Opioid Epidemic – A Call to
Action. N Engl J Med 2016; 375:2413-2415.
9. National Institute on Drug Abuse. (2007). Drugs,
Brains, and Behavior: The Science of Addiction. Retrieved from
https://d14rmgtrwzf5a.cloudfront.net/sites/default/files/soa_2014.pdf.
Accessed October 23, 2017.
10. Volkow ND et al. Medication-Assisted Therapies —
Tackling the Opioid Overdose Epidemic. N Engl J Med. 2014 May
29;370(22):2063-6. doi: 10.1056/NEJMp1402780. Epub 2014 Apr
23.
11. Florence CS et al. The Economic Burden of Prescription
Opioid Overdose, Abuse, and Dependence in the United States, 2013. Medical Care.
54(10):901-906, Oct 2016.
DOI:1097/MLR.0000000000000625. PMID:
27623005.
12. White House Council of Economic Advisers. (2017). The
Underestimated Cost of the Opioid Crisis. Retrieved from
https://www.whitehouse.gov/sites/whitehouse.gov/files/images/The%20Underestimated%20Cost%20of%20the%20Opioid%20Crisis.pdf.
Accessed November 20,
2017.
13. American Psychiatric Association (2013). Diagnostic
and statistical manual of mental disorders (5th ed.). Arlington, VA: American Psychiatric
Publishing.
14. Centers for Disease Control and Prevention. (2017).
Prescription Opioid Overdose Data. Retrieved from:
https://www.cdc.gov/drugoverdose/data/overdose.html. Accessed
September 28, 2017.
15. United Nations Office on Drugs and Crime, World Drug
Report 2017 (ISBN: 978-92-1-148291-1, eISBN: 978-92-1-060623-3,
United Nations publication, Sales No. E.17.XI.6).
SUBLOCADE is a trademark of Indivior UK Limited.
© Indivior PLC | INDIVIOR is a registered trademark of Indivior UK
Limited | All rights reserved
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