Multiple myeloma

Active Ingredient: Bendamustine

Indication for Bendamustine

Population group: only adults (18 years old or older)

Front line treatment of multiple myeloma (Durie-Salmon stage II with progress or stage III) in combination with prednisone for patients older than 65 years who are not eligible for autologous stem cell transplantation and who have clinical neuropathy at time of diagnosis precluding the use of thalidomide or bortezomib containing treatment.

For this indication, competent medicine agencies globally authorize below treatments:

120-150 mg/m² once a day for 2 days

Route of admnistration

Intravenous

Defined daily dose

120 - 150 mg per m² of body surface area (BSA)

Dosage regimen

From 120 To 150 mg per m² of body surface area (BSA) once every day for 2 day(s)

Detailed description

120-150 mg/m² body surface area bendamustine hydrochloride on days 1 and 2, 60 mg/m² body surface area prednisone i.v. or per os on days 1 to 4; every 4 weeks for at least 3 times.

Dosage considerations

For intravenous infusion over 30-60 min.

Active ingredient

Bendamustine

Bendamustine is an alkylating antitumour agent with unique activity. The antineoplastic and cytocidal effect of bendamustine is based essentially on a cross-linking of DNA single and double strands by alkylation. As a result, DNA matrix functions and DNA synthesis and repair are impaired.

Read more about Bendamustine

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