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|Updated Data with Oral Proteasome Inhibitor MLN9708 Reported in Newly Diagnosed Multiple Myeloma Patients|
− Oral Data Presentation to be Featured in "Highlights of ASH" −
New Orleans, LA, Dec. 9, 2013 and Osaka, Dec. 10, 2013 – Takeda Pharmaceutical Company Limited (TSE:4502) today announced final Phase 1 and preliminary Phase 2 results of a study combining oral investigational MLN9708 administered twice a week with lenalidomide and dexamethasone in patients with newly diagnosed multiple myeloma (MM). The investigators reported a combined complete response and very good partial response (CR+VGPR) rate of 76 percent (46/62) and a 94 percent overall response rate (ORR; 58/62 ≥ partial response). Stringent complete response (sCR) was reached in 75 percent of patients that attained CR. Overall, drug-related serious adverse events (SAEs) were reported in 28 percent of patients (18/64), and drug-related grade 3 adverse events (AEs) in 58 percent of patients (37/64). There were no drug-related grade 4 AEs. These data were presented today at the 55th American Society of Hematology (ASH) annual meeting held December 7-10 in New Orleans, LA.
"This all-oral MLN9708, lenalidomide and dexamethasone study generated high response rates and increased depth of response with extended treatment duration in newly diagnosed multiple myeloma patients," said lead investigator, Paul G. Richardson, MD, Dana-Farber Cancer Institute, Boston, MA. "This is the first all-oral proteasome inhibitor, IMiD combination under investigation in this setting to date, and the data support its feasibility and activity."
"The safety profile and encouraging response rates presented at ASH for the twice-a-week oral MLN9708 combination supplement our clinical understanding of this all-oral triplet regimen in newly diagnosed multiple myeloma patients," said Michael Vasconcelles, MD, Head, Oncology Therapeutic Area Unit. "Bringing new therapies to patients is an important goal, and the oral MLN9708 combination has the potential to become yet another way to extend proteasome inhibition. Based on data from this and another Phase 1/2 study, we are further exploring oral MLN9708 in our TOURMALINE Phase 3 development program using a once-a-week dosing schedule."
MLN9708 is an investigational, oral proteasome inhibitor being developed for the treatment of patients with MM and Amyloid Light-chain (AL) Amyloidosis. It is the first oral proteasome inhibitor to enter Phase 3 clinical trials.
Twice-Weekly Oral MLN9708, an Investigational Proteasome Inhibitor, in Combination with Lenalidomide (Len) and Dexamethasone (Dex) in Patients (Pts) with Newly Diagnosed Multiple Myeloma (MM): Final Phase 1 Results and Phase 2 Data (Abstract #535)
This oral presentation provides final Phase 1 results and Phase 2 data of a Phase 1/2 study. The primary objective of Phase 1 was to determine the safety, tolerability, maximum tolerated dose (MTD) and recommended Phase 2 dose; the primary objective of Phase 2 was to determine response rates (CR+VGPR) and further evaluate safety and tolerability. In this Phase 1/2 study, patients received MLN9708, lenalidomide and dexamethasone for up to 16, 21-day cycles, followed by MLN9708 maintenance until disease progression or unacceptable toxicity. Transplant-eligible patients could undergo stem cell collection after at least four cycles, and discontinue for autologous stem cell transplant (ASCT) after at least eight cycles. Key findings from the study, which were presented by Paul G. Richardson, MD, include:
At data cut-off, 33 percent (21/64) of patients overall discontinued to undergo ASCT, a further 17 percent (11/64) discontinued due to AEs, 9 percent (6/64) due to progressive disease and 16 percent (10/64) for other reasons.
About Multiple Myeloma
1"SEER Stat Fact Sheets: Myeloma." National Cancer Institute. http://seer.cancer.gov/statfacts/html/mulmy.html Last accessed November 21, 2013.
2"Cancer Facts & Figures 2013." American Cancer Society. 2013. http://www.cancer.org/acs/groups/content/@epidemiologysurveilance/documents/document/acspc-036845.pdf. Last accessed November 20,2013. Page 4.3Becker N. (2011). Epidemiology of Multiple Myeloma. In T. Moehler, H. Goldschmidt (Eds.), Multiple Myeloma. (p. 25). New York: Springer-Verlag Berlin Heidelberg. (Available online: http://rd.springer.com/chapter/10.1007%2F978-3-540-85772-3_2#page-1)