Examples of using Bendamustine in English and their translations into German
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Colloquial
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Official
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Ecclesiastic
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Medicine
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Financial
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Political
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Computer
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Programming
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Official/political
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Political
See section 5.1 for information on bendamustine dose.
Following treatment with bendamustine Gazyvaro is then used on its own for the maintenance treatment of FL.
Continue phase 3 study evaluating tafasitamab plus bendamustine in r/r DLBCL.
In direct comparisons, bendamustine has been proven to be superior to chlorambucil in terms of remission rate, the rate of complete remissions and progression-free survival 13.
The recommended dose of Gazyvaro in combination with bendamustine is shown in Table 4.
Patients were randomized 1:1 to receive either bendamustine(B) alone(n 202) or Gazyvaro in combination with bendamustine(G+B)(n 194) for 6 cycles, each of 28 days duration.
Ofatumumab is administered intravenously andis approved for first-line therapy in combination with bendamustine.
Chlorambucil, fludarabine-containing regimens, bendamustine, also in combination with rituximab.
On the basis of additional Phase II study data, ofatumumab has received approval as afirst line therapy in combination with chlorambucil or bendamustine.
Gazyvaro+ chlorambucil or Gazyvaro+ bendamustine(induction) followed by Gazyvaro maintenance.
Patients received Arzerra as monthly intravenous infusions(Cycle 1 300 mg on day 1 and 1,000 mg on day 8, subsequent cycles: 1,000 mg on day 1 every 28 days)in combination with intravenous bendamustine 90 mg/m2 at days 1 and 2 every 28 days.
The results of this study demonstrated that Arzerra in combination with bendamustine is an effective therapy providing an ORR of 95%(95% CI: 85, 99) and a CR of 43.
A third study, in 578 patients whose disease had not responded or had come back after previous treatment, compared adding Imbruvica or placebo(a dummy treatment)to the cancer medicines bendamustine and rituximab.
The combination of obinutuzumab with chlorambucil or bendamustine may increase neutropenia see section 4.4.
The primary analysis based on independent Review Committee(IRC) assessment demonstrated a statistically significant- 45% reduction in the risk of disease progression(PD) or death, in patients with iNHL receiving G+B followed by Gazyvaro maintenance,compared with patients receiving bendamustine alone.
In summary,comorbid patients as well should receive treatment with bendamustine in combination with rituximab or ofatumumab, or with chlorambucil in combination with rituximab and ofatumumab or obinutuzumab.
The study showed that people lived significantly longer without disease worsening or death(progression-free survival, PFS) when treated with Gazyva(obinutuzumab) plus bendamustine followed by Gazyva alone, compared to bendamustine alone.
Investigator-assessed median PFS with the GAZYVARO regimen was more than double that with bendamustine alone mPFS(investigator): GAZYVARO plus bendamustine 29.2 months vs. bendamustine alone 14 months, HR=0.52, 95 percent CI 0.39- 0.70, p< 0.0001.
The most common Grade 3-4 adverse events that occurred more often(at least 2 percent or greater) in those receiving the Gazyva/Gazyvaro plus bendamustine regimen compared to those receiving bendamustine alone were low white blood cell count neutropenia;
Title A phase I/II safety and efficacy trial of a combination of bendamustine, rituximab and lenalidomide(BRL) with relapsed or refractory chronic lymphocytic leukemia(CLL) and a phase II efficacy trial for patients with previously untreated CLL.
GADOLIN is a phase III open-label, multicentre, randomised two-arm study evaluating Gazyva/Gazyvaro plus bendamustine followed by Gazyva/Gazyvaro alone for up to two years, compared to bendamustine alone.
B-MIND: Continue the pivotal phase 3 study evaluating MOR208 plus bendamustine versus rituximab plus bendamustine in r/r DLBCL and conduct a pre-planned, event-driven, interim analysis of B-MIND, which is projected to take place in the second half of 2019.
GADOLIN(NCT01059630; GA04753g) is a phase III open-label, multicentre, randomised two-arm study evaluating Gazyva/Gazyvaro plus bendamustine followed by Gazyva/Gazyvaro alone until disease progression or for up to two years compared to bendamustine alone.
The B-MIND study is designed to investigate MOR208 in combination with the chemotherapeutic agent bendamustine in patients with relapsed/refractory DLBCL who are not eligible for high-dose chemotherapy(HDC) and autologous stem cell transplantation(ASCT) in comparison to the combination of the anti-CD20 antibody rituximab plus bendamustine.
For those who fail to achieve durable disease control with MabThera-based treatment,Gazyvaro plus bendamustine is an important new treatment option that has been shown to reduce the risk of disease progression or death by more than half.
Patients who respond to induction treatment(i.e. the initial 6 treatment cycles)with Gazyvaro in combination with bendamustine or have stable disease should continue to receive Gazyvaro 1,000 mg as single agent maintenance therapy once every 2 months for two years or until disease progression whichever occurs first.
In a subgroup analysis of people with follicular lymphoma, the most common type of iNHL, treatment with Gazyva®/Gazyvaro®(obinutuzumab) plus bendamustine provided significantly greater depth of remission at end of induction compared to bendamustine alone, as measured by minimal residual disease(MRD)-negativity(82% vs 43%, respectively; p< 0.0001)1.
GADOLIN(NCT01059630; GA04753g) is a Phase III open-label, multicenter, randomized two-arm study evaluating Gazyva plus bendamustine followed by Gazyva alone for up to two years compared to bendamustine alone in 413 patients with indolent non-Hodgkin's lymphoma whose disease progressed during or following MabThera/Rituxan-based therapy.
This communication contains certain forward-looking statements concerning the MorphoSys group of companies, including the expectations regarding the clinical development of tafasitamab in combination with bendamustine versus rituximab and bendamustine in the B-MIND study in r/r DLBCL, the further clinical development of tafasitamab as well as interactions with regulatory authorities and expectations regarding regulatory filings and possible approvals for tafasitamab.