Articles tagged with: Elotuzumab
News»

The main multiple myeloma-related poster session at this year's American Society of Clinical Oncology (ASCO) annual meeting in Chicago took place last Monday. Several of the posters presented during that session focused on potential new multiple myeloma therapies. Those posters were reviewed in the Beacon's previous ASCO multiple myeloma update.
In this, the Beacon's final ASCO 2016 update, the attention shifts to posters from the Monday session that were related to existing myeloma therapies, as well as a pair of posters related to smoldering multiple myeloma.
The posters about existing therapies …
Deutsch»

Die Europäische Arzneimittelkommission hat Empliciti (Elotuzumab) für die Behandlung des multiplen Myeloms zugelassen.
Die Zulassung bedeutet, dass Myelompatienten in Europa mit Empliciti behandelt werden können, ohne sich in eine klinische Studie einschreiben zu müssen.
Die europäische Zulassung von Empliciti folgt der Zulassung in den Vereinigten Staaten im letzten November, dem Markt, auf dem das Medikament seine allererste Zulassung erhalten hat. Wie in den Vereinigten Staaten ist Empliciti in Europa für die Anwendung in Kombination mit Revlimid (Lenalidomid) und Dexamethason zugelassen worden.
Genauer gesagt ist die europäische Zulassung von Empliciti für die Anwendung …
News»

The European Commission has approved Empliciti (elotuzumab) for the treatment of multiple myeloma.
The approval means that myeloma patients in Europe will now be able to be treated with Empliciti without having to enroll in a clinical trial.
Empliciti's European approval comes on the heals of its approval late last November in the United States, the market in which the drug received its first ever regulatory approval. As in the United States, Empliciti has been approved in Europe for use in combination with Revlimid (lenalidomide) and dexamethasone.
More …
Press Releases»
First and only immunostimulatory antibody approved in the European Union for multiple myeloma
Accelerated assessment and approval based on long-term data from ELOQUENT-2, which evaluated Empliciti in combination with Revlimid® (lenalidomide) and dexamethasone (Rd)
ELOQUENT-2 demonstrated the Empliciti combination delivered a 53% relative improvement in progression-free survival vs. Rd alone at three years (23% vs. 15%)
Princeton, NJ (Press Release) – Bristol-Myers Squibb Company (NYSE:BMY) and AbbVie (NYSE:ABBV) announced today that the European Commission has approved Empliciti™ (elotuzumab) for the treatment of multiple myeloma as combination therapy with Revlimid® (lenalidomide) and dexamethasone in patients who have received at least one prior therapy. Empliciti is now the first and only immunostimulatory antibody approved for multiple myeloma in the European Union (EU).
The approval is based on data from the randomized, open-label, Phase 3 ELOQUENT-2 study, which evaluated Empliciti in …
News»

A happy Tuesday to you, myeloma world.
We have some interesting research to share with you.
First, we have results of a Phase 2 study investigating Empliciti (elotuzumab) in combination with Velcade (bortezomib) and dexamethasone (Decadron) in relapsed and refractory myeloma patients. The results show that Empliciti plus Velcade and dexamethasone improves progression-free survival compared to Velcade and dexamethasone alone, without adding any significant side effects.
We also report on a study out of Italy that explores using Treanda (bendamustine) in addition to melphalan (Alkeran) as the high-dose chemotherapy …
Opinion»

As I mentioned in my previous column, I started treatment with the newly approved myeloma drug Empliciti (elotuzumab) in February. I thought I would share more details about my experiences with the drug so far.
Before I started treatment with Empliciti, I had enjoyed a drug holiday for the previous three months. I appreciated the break from the side effects of drugs and numerous trips to the cancer center.
Before the drug holiday, I was on Kyprolis (carfilzomib), Revlimid (lenalidomide) and dexamethasone (Decadron) for …
News, Opinion»

What a year 2015 was for the myelomatologist!
The U.S. Food and Drug Administration (FDA) approval of three new myeloma drugs, all within the span of a few weeks towards the end of the year, had already generated great excitement in the community.
Then, several potential practice-changing presentations at the 2015 American Society of Hematology (ASH) annual meeting put the proverbial icing on the cake to round out a landmark year for myeloma therapeutics.
This edition of the myeloma quiz highlights some of the key takeaways from the ASH 2015 meeting.
- …