Decision Marks Latest Once-Daily, Oral Treatment of Thrombocytopenia in Adults with Chronic Liver Disease Scheduled to Undergo a Procedure
OSAKA, Japan & FLORHAM PARK, NJ, USA I August 01, 2018 I Shionogi & Co., Ltd. (hereafter “Shionogi”) announced today that, after completing a Priority Review, the U.S. Food and Drug Administration (FDA) has approved Mulpleta® (lusutrombopag), a once-daily, orally administered, small molecule thrombopoietin (TPO) receptor agonist for the treatment of thrombocytopenia in adult patients with chronic liver disease (CLD) who are scheduled to
“We are very pleased the FDA has approved Mulpleta as a new, safe and effective treatment,” said Takayuki Yoshioka, President and Chief Executive Officer, Shionogi Inc. “This new therapy offers physicians and patients another choice beyond platelet transfusions as adult patients with CLD often undergo procedures that could put them at increased risk for bleeding.”
The FDA approval was based on consistent safety and efficacy data from two Phase 3 clinical trials, L-PLUS 1 and L-PLUS 2, in which Mulpleta met primary and secondary endpoints with statistically significant results.
“Therapeutic options in this area are critically needed, as adult patients with chronic liver disease often require multiple procedures for various medical reasons,” said Dr. Nezam Afdhal, Senior Physician in Hepatology at Beth Israel Deaconess Medical Center and Professor of Medicine at Harvard Medical School. “I look forward to being able to offer this new oral treatment to patients, instead of relying solely on platelet transfusion.”
About Thrombocytopenia in Chronic Liver Disease
Thrombocytopenia is a common complication of CLD, which may be caused by multiple factors including decreased production of TPO. Thrombocytopenia is frequently observed in patients with CLD, with studies suggesting that it occurs in up to 78% of patients with cirrhosis.1 CLD-associated thrombocytopenia is defined as a platelet count of less than 150,000/µL and is the most common hematologic complication of CLD.2,3,4 Patients with CLD and thrombocytopenia are at increased risk for bleeding, requiring recurrent platelet transfusions, increased ambulatory visits and inpatient hospital stays compared with patients with CLD without thrombocytopenia.5 The annual health care cost of a patient with CLD with thrombocytopenia is more than three times that of a patient with CLD without thrombocytopenia.5 In addition to the potential of thrombocytopenia, especially severe thrombocytopenia (platelet count less than 50,000/µL), to aggravate surgical or traumatic bleeding, it may also significantly complicate routine diagnostic procedures and patient care, such as liver biopsy and medically indicated or elective procedures for cirrhotic patients, resulting in delayed or cancelled curative treatment.6
About Mulpleta
Mulpleta (lusutrombopag) is a once-daily, orally administered, small molecule TPO receptor agonist for the treatment of thrombocytopenia in adult patients with CLD who are scheduled to undergo a procedure. Lusutrombopag is an orally bioavailable, small molecule TPO receptor agonist that interacts with the transmembrane domain of human TPO receptors expressed on megakaryocytes to induce the proliferation and differentiation of megakaryocytic progenitor cells from hematopoietic stem cells and megakaryocyte maturation.
Mulpleta was approved by the Ministry of Health, Labor and Welfare in Japan in September 2015 for the improvement of thrombocytopenia associated with CLD in patients undergoing an elective invasive procedure. The European Medicines Agency has validated for review Shionogi’s standard Marketing Authorization Application for lusutrombopag and approval is expected in 1H 2019.
In the U.S., Mulpleta is expected to be available by early September 2018.
Please see Important Safety Information, including Warnings & Precautions and Adverse Reactions below.
INDICATION
Mulpleta® (lusutrombopag) is indicated for the treatment of thrombocytopenia in adult patients with chronic liver disease who are scheduled to undergo a procedure.
About Shionogi
Shionogi & Co., Ltd. is a major research-driven pharmaceutical company dedicated to bringing benefits to patients based on its corporate philosophy of “supplying the best possible medicine to protect the health and wellbeing of the patients we serve.” Shionogi’s research and development currently target two therapeutic areas: infectious diseases, and pain/CNS disorders. For over 50 years, Shionogi has developed and commercialized innovative oral and parenteral anti-infectives. In addition, Shionogi is engaged in new research areas, such as obesity/geriatric metabolic disease and oncology/immunology. Contributing to the health and quality of life of patients around the world through development in these therapeutic areas is Shionogi’s primary goal. For more details, please visit www.shionogi.co.jp/en/. For more information on Shionogi Inc., the U.S.–based subsidiary of Shionogi & Co., Ltd., headquartered in Florham Park, NJ, USA, please visit www.shionogi.com. For more information on Shionogi Ltd., the UK-based subsidiary of Shionogi & Co. Ltd., headquartered in London, England, please visit www.shionogi.eu.
| References: |
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Peck-Radosavljevic M. Liver Int. 2017; 37(6):778-793. |
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2. |
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Giannini EG. Aliment Pharmacol Ther. 2006; 23(8):1055-1065. |
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3. |
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Koruk M, et al. Hepatogastroenterology. 2002; 49(48):1645-1648. |
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4. |
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Aref S, et al. Hematology. 2004; 9(5/6):351-356. |
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5. |
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Poordad F, et al. J Med Econ. 2012; 15:112-124. |
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6. |
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Hayashi H, et al. World J Gastroenterol. 2014; 20: 2595-2605. |
SOURCE: Shionogi
Post Views: 35
Decision Marks Latest Once-Daily, Oral Treatment of Thrombocytopenia in Adults with Chronic Liver Disease Scheduled to Undergo a Procedure
OSAKA, Japan & FLORHAM PARK, NJ, USA I August 01, 2018 I Shionogi & Co., Ltd. (hereafter “Shionogi”) announced today that, after completing a Priority Review, the U.S. Food and Drug Administration (FDA) has approved Mulpleta® (lusutrombopag), a once-daily, orally administered, small molecule thrombopoietin (TPO) receptor agonist for the treatment of thrombocytopenia in adult patients with chronic liver disease (CLD) who are scheduled to
“We are very pleased the FDA has approved Mulpleta as a new, safe and effective treatment,” said Takayuki Yoshioka, President and Chief Executive Officer, Shionogi Inc. “This new therapy offers physicians and patients another choice beyond platelet transfusions as adult patients with CLD often undergo procedures that could put them at increased risk for bleeding.”
The FDA approval was based on consistent safety and efficacy data from two Phase 3 clinical trials, L-PLUS 1 and L-PLUS 2, in which Mulpleta met primary and secondary endpoints with statistically significant results.
“Therapeutic options in this area are critically needed, as adult patients with chronic liver disease often require multiple procedures for various medical reasons,” said Dr. Nezam Afdhal, Senior Physician in Hepatology at Beth Israel Deaconess Medical Center and Professor of Medicine at Harvard Medical School. “I look forward to being able to offer this new oral treatment to patients, instead of relying solely on platelet transfusion.”
About Thrombocytopenia in Chronic Liver Disease
Thrombocytopenia is a common complication of CLD, which may be caused by multiple factors including decreased production of TPO. Thrombocytopenia is frequently observed in patients with CLD, with studies suggesting that it occurs in up to 78% of patients with cirrhosis.1 CLD-associated thrombocytopenia is defined as a platelet count of less than 150,000/µL and is the most common hematologic complication of CLD.2,3,4 Patients with CLD and thrombocytopenia are at increased risk for bleeding, requiring recurrent platelet transfusions, increased ambulatory visits and inpatient hospital stays compared with patients with CLD without thrombocytopenia.5 The annual health care cost of a patient with CLD with thrombocytopenia is more than three times that of a patient with CLD without thrombocytopenia.5 In addition to the potential of thrombocytopenia, especially severe thrombocytopenia (platelet count less than 50,000/µL), to aggravate surgical or traumatic bleeding, it may also significantly complicate routine diagnostic procedures and patient care, such as liver biopsy and medically indicated or elective procedures for cirrhotic patients, resulting in delayed or cancelled curative treatment.6
About Mulpleta
Mulpleta (lusutrombopag) is a once-daily, orally administered, small molecule TPO receptor agonist for the treatment of thrombocytopenia in adult patients with CLD who are scheduled to undergo a procedure. Lusutrombopag is an orally bioavailable, small molecule TPO receptor agonist that interacts with the transmembrane domain of human TPO receptors expressed on megakaryocytes to induce the proliferation and differentiation of megakaryocytic progenitor cells from hematopoietic stem cells and megakaryocyte maturation.
Mulpleta was approved by the Ministry of Health, Labor and Welfare in Japan in September 2015 for the improvement of thrombocytopenia associated with CLD in patients undergoing an elective invasive procedure. The European Medicines Agency has validated for review Shionogi’s standard Marketing Authorization Application for lusutrombopag and approval is expected in 1H 2019.
In the U.S., Mulpleta is expected to be available by early September 2018.
Please see Important Safety Information, including Warnings & Precautions and Adverse Reactions below.
INDICATION
Mulpleta® (lusutrombopag) is indicated for the treatment of thrombocytopenia in adult patients with chronic liver disease who are scheduled to undergo a procedure.
About Shionogi
Shionogi & Co., Ltd. is a major research-driven pharmaceutical company dedicated to bringing benefits to patients based on its corporate philosophy of “supplying the best possible medicine to protect the health and wellbeing of the patients we serve.” Shionogi’s research and development currently target two therapeutic areas: infectious diseases, and pain/CNS disorders. For over 50 years, Shionogi has developed and commercialized innovative oral and parenteral anti-infectives. In addition, Shionogi is engaged in new research areas, such as obesity/geriatric metabolic disease and oncology/immunology. Contributing to the health and quality of life of patients around the world through development in these therapeutic areas is Shionogi’s primary goal. For more details, please visit www.shionogi.co.jp/en/. For more information on Shionogi Inc., the U.S.–based subsidiary of Shionogi & Co., Ltd., headquartered in Florham Park, NJ, USA, please visit www.shionogi.com. For more information on Shionogi Ltd., the UK-based subsidiary of Shionogi & Co. Ltd., headquartered in London, England, please visit www.shionogi.eu.
| References: |
| |
|
|
1. |
|
Peck-Radosavljevic M. Liver Int. 2017; 37(6):778-793. |
| |
|
|
2. |
|
Giannini EG. Aliment Pharmacol Ther. 2006; 23(8):1055-1065. |
| |
|
|
3. |
|
Koruk M, et al. Hepatogastroenterology. 2002; 49(48):1645-1648. |
| |
|
|
4. |
|
Aref S, et al. Hematology. 2004; 9(5/6):351-356. |
| |
|
|
5. |
|
Poordad F, et al. J Med Econ. 2012; 15:112-124. |
| |
|
|
6. |
|
Hayashi H, et al. World J Gastroenterol. 2014; 20: 2595-2605. |
SOURCE: Shionogi
Post Views: 35
