Libtayo is the third anti-PD-1 approved in the U.S.
CSCC is the second most common skin cancer in the U.S.
PARIS AND TARRYTOWN, NY – September 28, 2018 – The U.S. Food and Drug
Administration (FDA) has approved Libtayo®
(cemiplimab-rwlc) for the treatment of
patients with metastatic cutaneous squamous cell carcinoma (CSCC) or locally advanced
CSCC who are not candidates for curative surgery or curative radiation. Libtayo is a fullyhuman monoclonal antibody targeting the immune checkpoint receptor PD-1
(programmed cell death protein-1) and is the first and only treatment specifically
approved and available for advanced CSCC in the U.S.
“Today’s FDA decision is great news for patients with advanced CSCC, who
previously had no approved treatment options. This is especially true because
these patients are no longer candidates for curative surgery or radiation,” said
Michael R. Migden, M.D., a lead investigator in the pivotal CSCC clinical program
and Professor in the Departments of Dermatology and Head and Neck Surgery at
The University of Texas MD Anderson Cancer Center. “Libtayo is an important
new immunotherapy option for U.S. physicians to help address a significant
unmet need in this patient group.”
CSCC is the second most common form of skin cancer and is responsible for an
estimated 7,000 deaths each year in the U.S. It currently accounts for approximately 20
percent of all skin cancers in the U.S., with the number of newly diagnosed cases
expected to rise annually. When CSCC invades deeper layers of the skin or adjacent
tissues, it is categorized as locally advanced. Once it spreads to other distant parts of
the body, it is considered metastatic.
“By following the science, we identified early on that advanced CSCC was a
promising target for investigation with Libtayo,” said Israel Lowy, M.D., Ph.D.,
Vice President of Global Clinical Development and Head of Translational Science
and Clinical Oncology, Regeneron. “We are proud to offer patients in the U.S. this
first and only treatment for advanced CSCC and remain focused on advancing
our clinical research investigating Libtayo as a potential monotherapy and
combination therapy in other cancer types.”
Libtayo was evaluated by the FDA under Priority Review, which is reserved for
medicines that represent significant improvements in safety or efficacy in treating
serious conditions, and in 2017 was granted Breakthrough Therapy Designation status
for advanced CSCC. Breakthrough Therapy Designation was created to expedite the
development and review of drugs that have the potential for substantial improvement in
the treatment of serious or life-threatening conditions.
“In the U.S., CSCC accounts for one in five skin cancers, and the number of new
diagnoses is increasing,” said Olivier Brandicourt, M.D., Chief Executive Officer,
Sanofi. “We believe Libtayo has the potential to make a difference for U.S.
patients with advanced CSCC, as it helps to fill a critical gap in treatment options.
We are committed to bringing this important medicine to patients in other
countries around the world as quickly as possible.”
The recommended dosage of Libtayo is 350 mg administered as an intravenous infusion
over 30 minutes every three weeks, until disease progression or unacceptable toxicity.
Libtayo is available as a single-dose 350 mg vial.
Libtayo is expected to provide significant value for patients with advanced CSCC and
those who care for them. The U.S. list price, or wholesale acquisition cost, is $9,100 per
three-week treatment cycle. Actual costs to patients are generally anticipated to be lower
as the list price does not reflect insurance coverage, copay support, or financial
assistance from patient support programs.
Sanofi and Regeneron are committed to helping U.S. patients who have been
prescribed Libtayo access their medication. The companies have launched Libtayo
Surround™ to help patients understand how Libtayo may be covered by their health
insurance plans. Additionally, Libtayo Surround is designed to help eligible patients who
need financial assistance with their prescription. For more information, please call 1-877-
LIBTAYO (1-877-542-8296), Option 1, or visit www.Libtayo.com.
Sanofi Genzyme, the specialty care global business unit of Sanofi, and Regeneron will
market Libtayo jointly in the U.S.
Pivotal advanced CSCC clinical program and results
The FDA approval of Libtayo was based on a combined analysis of data from an openlabel, multi-center, non-randomized Phase 2 trial known as EMPOWER-CSCC-1 (Study
1540) and two advanced CSCC expansion cohorts from a multi-center, open-label, nonrandomized Phase 1 trial (Study 1423). Together, the trials represent the largest
prospective data set in advanced CSCC.
The major efficacy outcome measures for the integrated analysis of EMPOWER-CSCC1 and the two CSCC expansion cohorts were confirmed objective response rate (ORR),
as assessed by independent central review (ICR), and ICR-assessed duration of
response (DOR). The efficacy analysis was conducted when all patients had the
opportunity for at least six months of follow-up.
Combined efficacy results (n=108) from EMPOWER-CSCC-1 and the two advanced
CSCC expansion cohorts from the Phase 1 trial were as follows:
Efficacy Endpoints* Metastatic
†Only includes patients with complete healing of prior cutaneous involvement; locally advanced CSCC
patients in EMPOWER-CSCC-1 required biopsy to confirm complete response.
For the combined safety analysis (n=163) of EMPOWER-CSCC-1 and the two advanced
CSCC expansion cohorts, the most common adverse reactions reported were fatigue
(29%), rash (25%) and diarrhea (22%). Libtayo was permanently discontinued due to
adverse reactions in 5% of patients; adverse reactions resulting in permanent
discontinuation were pneumonitis, autoimmune myocarditis, hepatitis, aseptic
meningitis, complex regional pain syndrome, cough and muscular weakness. Serious
adverse reactions (SAEs) occurred in 28% of patients. SAEs that occurred in at least 2%
of patients were cellulitis, sepsis, pneumonia, pneumonitis and urinary tract infection.
Cemiplimab-rwlc development program overview
Cemiplimab-rwlc is being jointly developed by Regeneron and Sanofi under a global
In April 2018, the European Medicines Agency (EMA) accepted for review the Marketing
Authorization Application for Libtayo for the treatment of patients with metastatic CSCC
or with locally advanced CSCC who are not candidates for surgery. The EMA review
process is anticipated to be complete in the first half of 2019. There are currently no
EMA-approved treatments for advanced CSCC. Regulatory applications in additional
countries are also being considered for submission later in 2018.
In addition to advanced CSCC, cemiplimab-rwlc is being investigated in trials in nonsmall cell lung cancer, basal cell carcinoma, and cervical cancer along with trials in
squamous cell carcinoma of the head and neck, melanoma, colorectal cancer, prostate
cancer, multiple myeloma, Hodgkin lymphoma and non-Hodgkin lymphoma. These
potential uses are investigational, and their safety and efficacy have not been evaluated
by any regulatory authority.
IMPORTANT SAFETY INFORMATION AND INDICATION FOR U.S. PATIENTS
What is the most important information I should know about Libtayo?
Libtayo is a medicine that may treat a type of skin cancer by working with your immune
system. Libtayo can cause your immune system to attack normal organs and tissues in
any area of your body and can affect the way they work. These problems can
sometimes become severe or life-threatening and can lead to death. These problems
may happen anytime during treatment or even after your treatment has ended.
Call or see your healthcare provider right away if you develop any symptoms of
the following problems or these symptoms get worse:
Lung problems (pneumonitis). Signs and symptoms of pneumonitis may include
new or worsening cough, shortness of breath, and chest pain.
Intestinal problems (colitis) that can lead to tears or holes in your intestine.
Signs and symptoms of colitis may include diarrhea (loose stools) or more frequent
bowel movements than usual; stools that are black, tarry, or sticky or that have blood
or mucus; and severe stomach-area (abdomen) pain or tenderness.
Liver problems (hepatitis). Signs and symptoms of hepatitis may include yellowing
of your skin or the whites of your eyes, severe nausea or vomiting, pain on the right
side of your stomach area (abdomen), drowsiness, dark urine (tea colored), bleeding
or bruising more easily than normal, and feeling less hungry than usual.
Hormone gland problems (especially the adrenal glands, pituitary, thyroid and
pancreas). Signs and symptoms that your hormone glands are not working properly
may include headaches that will not go away or unusual headaches, rapid heartbeat,
increased sweating, extreme tiredness, weight gain or weight loss, dizziness or
fainting, feeling more hungry or thirsty than usual, hair loss, feeling cold, constipation,
deeper voice, very low blood pressure, urinating more often than usual, nausea or
vomiting, stomach-area (abdomen) pain, and changes in mood or behavior, such as
decreased sex drive, irritability, or forgetfulness.
Kidney problems, including nephritis and kidney failure. Signs of these problems
may include decrease in your amount of urine, blood in your urine, swelling in your
ankles, and loss of appetite.
Skin problems. Signs of these problems may include rash, itching, skin blistering,
and painful sores or ulcers in the mouth, nose, throat, or genital area.
Problems in other organs. Signs of these problems may include headache,
tiredness or weakness, sleepiness, changes in heartbeat (such as beating fast,
seeming to skip a beat, or a pounding sensation), confusion, fever, muscle
weakness, balance problems, nausea, vomiting, stiff neck, memory problems,
seizures (encephalitis), swollen lymph nodes, rash or tender lumps on skin, cough,
shortness of breath, vision changes, or eye pain (sarcoidosis), seeing or hearing
things that are not there (hallucinations), severe muscle weakness, low red blood
cells (anemia), bruises on the skin or bleeding, and changes in eyesight.
Rejection of a transplanted organ. Your doctor should tell you what signs and
symptoms you should report and monitor you, depending on the type of organ
transplant that you have had.
Infusion (IV) reactions that can sometimes be severe and life-threatening. Signs
of these problems may include chills or shaking, itching or rash, flushing, shortness
of breath or wheezing, dizziness, fever, feeling of passing out, back or neck pain, and
Getting medical treatment right away may help keep these problems from
becoming more serious.
Your healthcare provider will check you for these problems during your treatment with
Libtayo. Your healthcare provider may treat you with corticosteroid or hormone
replacement medicines. Your healthcare provider may delay or completely stop
treatment if you have severe side effects.
Before you receive Libtayo, tell your healthcare provider about all your medical
conditions, including if you:
• have immune system problems such as Crohn’s disease, ulcerative colitis, or lupus;
• have had an organ transplant;
• have lung or breathing problems;
• have liver or kidney problems;
• have diabetes;
• are pregnant or plan to become pregnant; Libtayo can harm your unborn baby
Females who are able to become pregnant:
o Your healthcare provider will give you a pregnancy test before you start
o You should use an effective method of birth control during your treatment and for
at least 4 months after your last dose of Libtayo. Talk with your healthcare
provider about birth control methods that you can use during this time.
o Tell your healthcare provider right away if you become pregnant or think you may
be pregnant during treatment with Libtayo.
• are breastfeeding or plan to breastfeed. It is not known if Libtayo passes into your
breast milk. Do not breastfeed during treatment and for at least 4 months after the
last dose of Libtayo.
Tell your healthcare provider about all the medicines you take, including
prescription and over-the-counter medicines, vitamins, and herbal supplements.
The most common side effects of Libtayo include tiredness, rash, and diarrhea. These
are not all the possible side effects of Libtayo. Call your doctor for medical advice about
side effects. You may report side effects to FDA at 1-800-FDA-1088. You may also
report side effects to Regeneron Pharmaceuticals and Sanofi at 1-877-542-8296.
Please see accompanying full Prescribing Information, including Medication
What is Libtayo?
Libtayo is a prescription medicine used to treat people with a type of skin cancer called
cutaneous squamous cell carcinoma (CSCC) that has spread or cannot be cured by
surgery or radiation.
It is not known if Libtayo is safe and effective in children.
About Regeneron Pharmaceuticals, Inc
Regeneron (NASDAQ: REGN) is a leading biotechnology company that invents lifetransforming medicines for people with serious diseases. Founded and led for 30 years
by physician-scientists, our unique ability to repeatedly and consistently translate
science into medicine has led to seven FDA-approved treatments and numerous product
candidates in development, all of which were homegrown in our laboratories. Our
medicines and pipeline are designed to help patients with eye diseases, allergic and
inflammatory diseases, cancer, cardiovascular and metabolic diseases, neuromuscular
diseases, infectious diseases and rare diseases.
Regeneron is accelerating and improving the traditional drug development process
through our proprietary VelociSuite®
technologies, such as VelocImmune® which
produces optimized fully-human antibodies, and ambitious research initiatives such as
the Regeneron Genetics Center, which is conducting one of the largest genetics
sequencing efforts in the world.
For additional information about the company, please visit www.regeneron.com or follow
@Regeneron on Twitter.
Sanofi is dedicated to supporting people through their health challenges. We are a