Myeloma UK Clinical Trial Network Opens Its Fifth Trial To Patient Recruitment
Edinburgh (Press Release) - Myeloma UK has opened MUK four to patient recruitment. It is the fifth trial in the last two years to open in the Myeloma UK Clinical Trial Network (CTN) which provides access to promising myeloma drugs and aims to accelerate the process for approving new drugs and making them available on the NHS.
MUK four is a Phase II trial to assess the efficacy, safety and tolerability of vorinostat in combination with Velcade® (bortezomib) and dexamethasone (VVD) in patients with relapsed or relapsed refractory myeloma. MUK four will recruit up to 68 patients. It has opened at The Royal Marsden Hospital (RMH), London and is due to open in a number of other hospitals across the UK in the coming weeks.
Myeloma UK Chief Executive, Eric Low said,
“MUK four will give patients with relapsed or relapsed refractory myeloma access to vorinostat in combination with an already powerful anti-myeloma treatment combination: Velcade and dexamethasone.”
MUK four Chief Investigator, Dr Faith Davies from the RMH said,
“HDAC inhibitors like vorinostat are showing potential in the treatment of myeloma. MUK four will provide an indication of the effectiveness of vorinostat in a setting that is relevant for UK patients. This is one of only a limited number of clinical trials involving vorinostat in the world and will have a significant impact on how vorinostat is used for myeloma patients in the future.”
Study detail
Vorinostat is an oral inhibitor of class I and II histone deacetylase (HDAC).
Vorinostat works by blocking the actions of proteins called histone deacetylases which are needed to enable cells to divide. Myeloma cells rely heavily on histone deacetylases to work properly for their growth and survival. Inhibiting histone deacetylases causes the myeloma cells to die.
Treatment consists of up to eight cycles of vorinostat in combination with Velcade and dexamethasone, followed by single agent vorinostat maintenance. Treatment will continue until disease progression or unacceptable toxicity.
For more information about MUK four or if you have any questions about the Myeloma UK Clinical Trial Network please call the Myeloma Infoline on 0800 980 3332.
Source: Myeloma UK.
Related Press Releases:
- Low-Cost Dexamethasone Reduces Death By Up To One Third In Hospitalised Patients With Severe Respiratory Complications Of COVID-19
- FDA Approves Daratumumab For Transplant-Eligible Multiple Myeloma
- Oncopeptides Starts The Phase 2 PORT Study Comparing Peripheral Versus Central Administration Of Melflufen And Dexamethasone In Multiple Myeloma
- Oncopeptides Initiates U.S. Expanded Access Program With Melflufen In Triple-Class Refractory Multiple Myeloma
- FDA Grants Priority Review Of Melflufen For Patients With Triple-Class Refractory Multiple Myeloma