Pixantrone (BBR 2778) Versus Other Chemotherapeutic Agents for Third-Line Single Agent Treatment of Patients With Relapsed Aggressive Non-Hodgkins Lymphoma: A Randomized, Controlled, Phase III Comparative Trial
Latest Information Update: 13 Oct 2020
At a glance
- Drugs Pixantrone (Primary) ; Etoposide; Etoposide; Gemcitabine; Ifosfamide; Mitoxantrone; Oxaliplatin; Rituximab; Vinorelbine
- Indications Anaplastic large cell lymphoma; Diffuse large B cell lymphoma; Follicular lymphoma; Non-Hodgkin's lymphoma; Peripheral T-cell lymphoma
- Focus Registrational; Therapeutic Use
- Acronyms EXTEND
- Sponsors CTI BioPharma
- 13 Jun 2019 According to a Servier media release, the EC approval is based on data from the global clinical development of PIXUVRI which included pivotal study (PIX301) and a further Phase III clinical study (PIX306) conducted to satisfy requirements of the conditional authorization.
- 13 Jun 2019 According to a Servier media release, the European Commission (EC) has approved the conversion of the conditional approval of PIXUVRI (pixantrone) into a standard marketing authorization as a single agent for the treatment of adult patients with multiply relapsed or refractory aggressive non-Hodgkin B-cell lymphoma.
- 09 Apr 2019 According to a Servier media release, the positive opinion from the CHMP is based on data from the global clinical development of PIXUVRI which included pivotal study (PIX301) and a further Phase III clinical study (PIX306) conducted to satisfy requirements of the conditional authorization.