Pirtobrutinib(Jaypirca)
Acetylcysteine Injection, FLUIMUCIL, Acetylcysteine InjectionAcetylcysteine Injection, FLUIMUCIL, Acetylcysteine InjectionAcetylcysteine Injection, FLUIMUCIL, Acetylcysteine Injection
Reference price:
Manufacturer:
Eli Lilly and Company
Formulation:
TABLET
Validity period:
24 months
Reminder: The outer packaging is for reference only, please purchase and use under the guidance of a pharmacist. For read by medical and pharmaceutical professionals only.

JAYPIRCA (Pirtobrutinib) is an oral kinase inhibitor specifically developed for the treatment of hematologic malignancies, such as mantle cell lymphoma. It functions by inhibiting Bruton's Tyrosine Kinase (BTK), a critical enzyme involved in the signaling pathways of B-cells, which play a key role in various B-cell malignancies, including MCL. By targeting BTK, JAYPIRCA disrupts the survival and proliferation of malignant B-cells, making it an effective option for patients with relapsed or refractory MCL.

Approved by the U.S. FDA in 2023, JAYPIRCA offers a therapeutic option for patients who have not achieved durable responses to prior lines of systemic therapy, including those who have been treated with other BTK inhibitors. This makes JAYPIRCA a valuable addition to the therapeutic armamentarium for managing challenging cases of MCL where treatment options are limited.

Generic name

Pirtobrutinib(Jaypirca)
English name
Pirtobrutinib
Alternative Names
Jaypirca
Drug prices
Indications

Adult patients with relapsed or refractory MCL after at least two prior systemic therapies, including a BTK inhibitor.

Adult patients with CLL/SLL who have received at least two prior lines of therapy, including a BTK inhibitor and a BCL-2 inhibitor.

These indications are approved under accelerated approval based on response rate.

Therapeutic Target
Bruton’s tyrosine kinase (BTK)
Active Ingredients
Pirtobrutinib
Dosage form
TABLET
specifications
50mg * 30 tablets/bottle,100mg * 60 tablets/bottle
Description
JAYPIRCA® is an oral small-molecule kinase inhibitor that selectively targets Bruton's Tyrosine Kinase (BTK). BTK is involved in the signaling pathway of B-cells, and its inhibition helps disrupt the growth and survival of B-cell malignancies. Pirtobrutinib is designed to bind reversibly to the active site of BTK, which allows for activity in patients who have developed resistance to covalent BTK inhibitors.
Dosage and Administration

Recommended dose: 200 mg orally once daily.

May be taken with or without food. Tablets must be swallowed whole with water; not to be cut, crushed, or chewed.

Dose modifications are required for severe renal impairment (eGFR 15–29 mL/min), concomitant use with strong CYP3A inhibitors or moderate CYP3A inducers, and in case of adverse reactions.

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