Mulpleta®

Product List

Product Overview
Guideline Recommendations
Academic Publications
Mulpleta®

Lusutrombopag Tablets

Original imported quality
The only platelet-boosting drug with child-resistant packaging, globally certified and recommended by guidelines.

The world's first approved platelet-boosting drug for thrombocytopenia in chronic liver disease.
Original imported quality
Rapid onset and potent efficacy
Takes effect in 3-5 days, reaches target platelet count in 5 days, with a response rate of 72.7% on and after day 8.

Doubles the maximum platelet count from baseline after treatment.
Rapid onset and potent efficacy
Lower costs and higher efficiency
The only TPO-RA proven to significantly reduce bleeding risk compared to placebo.

39% lower daily treatment cost than the national negotiation reference product, saving medical insurance funds and reducing patient burden.
Lower costs and higher efficiency
The following product information is intended for use by healthcare professionals only.
The following product may not have been approved and/or licensed for marketing in all countries where this website is accessible.
Mulpleta®
Directions for Use Download
(for medical professionals only)
Adverse Event Reporting

Email: pv@eddingpharm.com

Hotline: 0512-67611023

Product information stated by NMPA in Approved Drug Catalog of China.

【Name】

Generic Name:Lusutrombopag Tablets

Brand Name:MULPLETA®(稳可达®) 

Chinese Pinyin:Luqubopa Pian
【Ingredients】

Active Ingredient:  Vancomycin

Excipients:Mannitol, hydrochloric acid, water for injection, nitrogen gas.

【Appearance】

Tablets: 3 mg lusutrombopag as a light red, round, film-coated tablet debossed with the Shionogi trademark ( ) above

the identifier code “551” on one side and with a “3” on the other side. 

【Indications】
MULPLETA is a thrombopoietin receptor agonist indicated for the treatment of thrombocytopenia in adult patients with chronic liver disease who are scheduled to undergo a procedure.
【Specification】
3 mg
For detailed product information, please download the full package insert (PDF).


Directions for Use Download
(for medical professionals only)
Adverse Event Reporting

Email: pv@eddingpharm.com

Hotline: 0512-67611023

Guideline Recommendations
CSCO Guidelines for the Diagnosis and Treatment of Tumor Therapy-Induced Thrombocytopenia (2025)

Recommended lusutrombopag for tumor CTIT patients (Grade III recommendation, Category 2B evidence).

Guidelines for the Diagnosis and Treatment of Primary Liver Cancer (2025 Edition)

Patients with thrombocytopenia caused by chronic liver disease may use recombinant human thrombopoietin or thrombopoietin receptor agonists (such as avatrombopag, lusutrombopag) to increase platelet count according to clinical needs.

Chinese Expert Consensus on the Clinical Application of Thrombopoietin Receptor Agonists in the Perioperative Period of Liver Cancer (2025 Edition)

Recommendation 5: Lusutrombopag and avatrombopag are recommended for the treatment of perioperative thrombocytopenia in liver cancer patients. (Agreement rate: 100%)

Recommendation 7: For patients with mild to moderate renal or liver impairment, neither lusutrombopag nor avatrombopag requires dosage adjustment. Comprehensive assessment of potential therapeutic risks is required before administration in other special populations. (Agreement rate: 100%)

Practical Guidelines for the Clinical Management of Cirrhotic Thrombocytopenia (2024)

Recommendation 4: When cirrhotic patients with thrombocytopenia undergo invasive procedures, surgery, or anti-tumor drug therapy, recombinant human thrombopoietin (rhTPO) or thrombopoietin receptor agonists (TPO-RA) may be used according to the required platelet threshold to reduce bleeding risk. (C1)

Academic Publications
Lusutrombopag for thrombocytopenia in Chinese patients with chronic liver disease undergoing invasive procedures
Journal: Hepatology International
Year: 2022
Read More