Wednesday, September 13, 2017 2:48:34 AM
you will see this on page 80:
Study NCT01077518 COMPLEMENT A+B (COMB157E2301)
Indication: Refractory iNHL (3rd Line)
Phase: Phase 3A
Patients: 346
Primary Outcome Measures: Progression-free-survival following ofatumumab and
bendamustine combination therapy
Arms/Intervention:
• Ofatumumab and Bendamustine infusions
• Bendamustine infusion
Target Patients: Patients with indolent B-cell non-Hodgkin's lymphoma
unresponsive to rituximab or a rituximab-containing regimen
during or within six months of treatment
Expected Completion: Q4-2017
Publication: Targeting congress in Q2-2018 (tbc)
In another article from August, 2015:
Swiss drugs maker Novartis has bought the rights to a medication that could treat multiple sclerosis from British pharmaceutical giant GlaxoSmithKline in a deal worth up to $1bn (£637m).........
As part of the asset-swap, GSK formed a consumer health joint venture with Novartis, while at the same buying the Swiss company's vaccines business.
In turn, Novartis, which already boasts a substantial oncology portfolio, has bought GSK's cancer drugs.
For GSK, the complex deal is part of a strategy by chief executive Sir Andrew Witty to return the business to growth and reverse the trend of the past few years of falling revenues and profits.
Yet a different article states:
First-half 2016 net sales of Arzerra by Novartis were $24.8 million a decrease of 22%. Sales were negatively impacted by increased competition, primarily from Imbruvica (ibrutinib).
Yes, it's no wonder someone wants VSTM's stock price as low as possible. Because, after all, a buyout is based to an extent on the stock price. Who's going to gain by messing with VSTM's stock price (i.e. acquiring VSTM)?
1. Novartis (they paid $1 billion for a useless cancer drug). They're trying to make use of their $1 billion by using the drug for MS indications.
2. GSX - they sold Novartis the drug (probably knowing it was worthless? lol). They can now turn around and acquire a better drug, for the same price (or better).
3. If AbbVie doesn't want competition, they better pay up now or possibly face something bigger down the line.
BTW, AbbVie paid $21 billion to Pharmacyclics for IMBRUVICA (ibrutinib). Yes, IMBRUVICA has a number of indications and Pharmacyclics had a lot of promising items as well. But IMBRUVICA was their star and as I previously noted, as for efficacy:
Summary of ibrutinib vs ofatumumab:
1. ibrutinib (Imbruvica) was statistically superior.
2. ibrutinib's PFS was 9.4 months vs ofatumumab's 8.1 months. Ratio = 9.4/8.1 = 1.16
3. ibrutinib had an "overall" 57% reduction in the risk of progression/death.
Summary of Verasem's drug (duvelisib) vs ofatumumab:
1. duvelisib was statistically superior.
2. duvelisib's PFS is 13.3 months vs ofatumumab's 9.9 months. Ratio = 13.3/9.9 = 1.34
3. duvelisib had a 48% (unsure if "overall" or specific groups) reduction in the risk of progression/death.
Recent VSTM News
- Verastem Oncology Announces Appointment of John Hayslip, M.D., to Chief Medical Officer • Business Wire • 04/18/2024 08:05:00 PM
- Verastem Oncology Announces Inducement Grants Under Nasdaq Listing Rule 5635(c)(4) • Business Wire • 04/04/2024 11:30:00 AM
- Global Patient Survey Results Reveal Significant Negative Impact on Social, Emotional and Mental Well-Being for People Living with Low-Grade Serous Ovarian Cancer • Business Wire • 03/18/2024 11:00:00 AM
- Verastem Oncology Reports Fourth Quarter and Full Year 2023 Financial Results and Highlights Recent Business Updates • Business Wire • 03/14/2024 08:05:00 PM
- Form SC TO-I/A - Tender offer statement by Issuer: [Amend] • Edgar (US Regulatory) • 03/11/2024 09:07:54 PM
- Verastem Oncology Announces Multiple Oral Presentations at SGO 2024 Annual Meeting on Women’s Cancer that Highlight Advances in Low-Grade Serous Ovarian Cancer Research and Reinforce Commitment to Addressing Urgent Unmet Needs • Business Wire • 03/11/2024 11:30:00 AM
- Verastem Oncology Receives Orphan Drug Designation from FDA for Avutometinib Alone or in Combination With Defactinib in Recurrent Low-Grade Serous Ovarian Cancer • Business Wire • 03/05/2024 10:27:00 PM
- Verastem Oncology Announces Preclinical Presentations for New Oral G12D Inhibitor and for Avutometinib and Defactinib Combination as a Backbone of Therapy for RAS/MAPK Driven Cancers at AACR Annual Meeting 2024 • Business Wire • 03/05/2024 09:30:00 PM
- Form SC TO-I - Tender offer statement by Issuer • Edgar (US Regulatory) • 02/08/2024 09:22:55 PM
- Form SC 13G/A - Statement of acquisition of beneficial ownership by individuals: [Amend] • Edgar (US Regulatory) • 02/02/2024 02:49:16 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 01/29/2024 09:01:10 PM
- Verastem Oncology Outlines Key 2024 Strategic Priorities and Upcoming Catalysts for Advancing Avutometinib and Defactinib and Broader Pipeline in RAS Pathway-Driven Cancers • Business Wire • 01/29/2024 12:00:00 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 01/19/2024 12:54:28 PM
- Verastem Oncology Granted Fast Track Designation for Combination of Avutometinib and Sotorasib for the Treatment of KRAS G12C-Mutant Non-Small Cell Lung Cancer (NSCLC) • Business Wire • 01/18/2024 09:00:00 PM
- Verastem Oncology to Participate in the B. Riley Securities 4th Annual Oncology Conference • Business Wire • 01/11/2024 12:00:00 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 01/09/2024 09:03:59 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 01/08/2024 09:02:35 PM
- Verastem Oncology Announces Inducement Grants Under Nasdaq Listing Rule 5635(c)(4) • Business Wire • 01/05/2024 12:00:00 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 12/28/2023 09:04:11 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 12/21/2023 09:01:15 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 12/20/2023 09:01:23 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 12/20/2023 09:00:56 PM
- Form DEF 14A - Other definitive proxy statements • Edgar (US Regulatory) • 12/19/2023 09:01:19 PM
- Verastem Oncology Selects Oral KRAS G12D Inhibitor GFH375/VS-7375 as Lead Program in Discovery and Development Collaboration with GenFleet Therapeutics • Business Wire • 12/18/2023 12:00:00 PM
- Verastem Oncology Announces Initiation of a Confirmatory Phase 3 Trial of Avutometinib and Defactinib in Recurrent Low-Grade Serous Ovarian Cancer • Business Wire • 12/13/2023 12:00:00 PM
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