Netupitant-Palonosetron FDC Market Opportunities,
Demand and Forecasts, 2017 - 2027
April 2017
Report Id : REP-GB-3096
Status : Ongoing
Category : Healthcare, Pharmaceuticals & Medical Devices
©2015 Future Market Insights, All Rights Reserved
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Systematic Research Approach
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Netupitant-Palonosetron FDC Market Opportunities, Demand and
Forecasts, 2017 - 2027
Netupitant-Palonosetron is the first approved fixed dose combination drug for the prevention of
chemotherapy induced nausea and vomiting. Cancer is a leading cause of death worldwide, accounting
nearly 1.4 million new cases in 2012. The most common type of cancer is lung cancer accounting about
1.59 million deaths, globally. Other prominent cancers are liver cancer, breast cancer, stomach cancer,
esophageal and stomach cancer. In 2012, nearly 8.2 million deaths occurred from aforementioned
indication, globally. Cancer can be treated by surgery, chemotherapy, radiation therapy, hormone
therapy, targeted therapy, precision medicine and stem cell transplantation. The most common
treatment for cancer is chemotherapy; it uses drugs to kill cancer cells that cause pain and other
problems. Chemotherapy given before surgery and radiation therapy to make the tumor cell smaller is
known as neo-adjuvant chemotherapy and chemotherapy given after treatment with surgery or radiation
therapy is known as adjuvant chemotherapy.
Chemotherapy, not only kills the cancer cells but also attacks healthy cells that leads to side effects such
as fatigue, hair loss, nausea, and vomiting. Chemotherapy-Induced Nausea and Vomiting (CINV) is one of
the most serious side effects that is taken into account. Chemotherapy-induced nausea and vomiting are
classified as acute, that occurs within 24 hours of the treatment; anticipatory, that is triggered due to
some exposed stimuli; other are refractory; delayed and breakthrough. Incidence, timing, and intensity of
chemotherapy-induced nausea and vomiting vary on chemotherapeutic agents and patient factors. CINV
occurs in about 80% of patients and has a severe impact on patient’s life.
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Netupitant-Palonosetron FDC Market Opportunities, Demand and
Forecasts, 2017 - 2027
Fixes dose combination for the treatment of Chemotherapy-induced Nausea and Vomiting is said to be
effective and is expected to overcome the side-effects of chemotherapy. Netupitant – Palonosetron FDC
is approved by U.S Food and Drug Administration for the prevention of acute nausea and vomiting during
cancer treatment process. The therapeutic drug is the combination of two drugs, namely Netupitant and
Palonosetron. Palonosetron was approved by FDA in 2008. It is a serotonin subtype 3 (5-HT3) receptor
antagonis for the prevention of acute nausea and vomiting. Netupitant is a (NK1) receptor antagonist
given after the start of chemotherapy. Antiemetics are less effective in controlling nausea and vomiting
because the intensity is high than actual vomiting. Proper antiemetics can prevent CINV in about 60%70% of patients.
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Netupitant-Palonosetron FDC Market: Drivers and Restrains
According to Word Health Organization, it is estimated that by 2030, about 23.6 million new cases of
cancer will prevail worldwide. Netupitant-Palonosetron Fixed Dose Combination is expected to fulfill
unmet needs of the chemotherapy-induced nausea and vomiting therapeutics market. The fixed dose
combination studies has revealed positive results in clinical phase trials. The demand of this drug for
better treatment option by physician and patients will drive the market. Intense research and
development in cancer therapeutics, the rise in the incidence of cancer cases, increased preference
toward chemotherapy for the treatment of cancer and the use of chemotherapy in combination with
other cancer treatment are anticipated to fuel the growth of Netupitant-Palonosetron FDC Market.
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Netupitant-Palonosetron FDC Market Opportunities, Demand and
Forecasts, 2017 - 2027
Netupitant-Palonosetron FDC Market: Segmentation
The global Netupitant-Palonosetron FDC markethas been classified by distribution channel, and
geography.
Netupitant-Palonosetron FDC is an oral formulation with 300 mg netupitant/0.5 mg palonosetron.
Palonosetron is available in the market as a single agent while netupitant is a new therapeutic agent
available in combination with Palonosetron. Netupitant-Palonosetron fixed dose combination is likely to
overcome problems associated with chemotherapy treatment option available in the market currently.
Netupitant-Palonosetron FDC Market: Overview
Netupitant-Palonosetron FDC, a serotonin receptor antagonists and NK1 receptor antagonist. Serotonin
receptor antagonists blocks the binding of serotonin to its receptor, thus stopping the signal to the brain.
Based on the distribution channel the Netupitant-Palonosetron FDC Market is segmented into hospital
pharmacy, drug store, retail pharmacy, and online pharmacy. The rise in the incidence of cancer patient
population, funding by the governmental bodies for research and development on cancer therapeutics,
focus on acquisition and merger by various key manufacturers for product expansion and technology use
for drug development is attributed towards the growth of the target market.
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Netupitant-Palonosetron FDC Market Opportunities, Demand and
Forecasts, 2017 - 2027
Netupitant-Palonosetron FDC Market: Regional Overview
Region-wise, the global Netupitant-Palonosetron FDCMarket is classified into regions namely, North
America, Latin America, Western Europe, Eastern Europe, Asia-Pacific, Japan, Middle East and Africa.
More than 70% of world's cancer death occurs in Africa, Asia, and South America. Around 33% of cancer
cases worldwide are due to smoke and tobacco.
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Netupitant-Palonosetron FDC Market: Key Players
The market leader for Netupitant-Palonosetron FDC Market is Helsinn Birex Pharmaceuticals Ltd and
the drug is distributed and marketed by Eisai Inc.
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