BRENTFORD, UK (TheStreet) — Duchenne muscular dystrophy patients treated withGlaxoSmithKline’s (GSK_) experimental drug drisapersen have been hospitalized due to kidney toxicity and low platelet counts, according to a Glaxo scientist who spoke at a research meeting in Rome last Sunday.
Glaxo has disclosed some safety data from early-stage drisapersen clinical trials previously, mainly related to moderate cases of proteinuria (excess protein in the urine) and decreased thrombocytes, which play a role in blood clotting. However, the significance of the adverse events attributed to drisapersen, also known as GSK-2402968, escalated with Sunday’s disclosure of hospitalized patients.
Dr. Rohit Batta, global medical leader in Glaxo’s neuromuscular rare disease unit, said four Duchenne muscular dystrophy (DMD) patients treated with drisapersen required hospitalization due to thrombocytopenia and that “several” patients with “severe proteinuria” also required hospitalization.
Batta’s remarks were made during a presentation on Sunday, Feb. 24 at The XI International Conference on Duchenne Muscular Dystrophy. The conference was held in Rome and organized by Duchenne Parent Project Onlus, an Italian DMD advocacy group.
Batta provided no other information about the hospitalized drisapersen patients during his presentation. A Glaxo spokesperson contacted Wednesday confirmed Batta’s remarks and added the DMD patients hospitalized were all enrolled in the ongoing phase II and phase III clinical trials of drisapersen. The hospitalizations had occurred “over the last two years” and had been discussed at previous medical meetings.
Thrombocytopenia is a condition caused by a significant decrease in the number of platelets, which control blood clotting. Patients with thrombocytopenia are at increased risk for uncontrolled bleeding. Proteinuria is the presence of excess protein in urine. Severe proteinuria can be a sign of kidney damage.
The hospitalizations due to serious adverse events attributed to drisapersen need to be evaluated in the context of the severity of DMD — a rare, progressive, muscle-wasting disease that forces patients into wheelchairs in their teens and dead soon after. But if drisapersen is found to cause significant toxicity, the drug may fall behind competing DMD therapies with cleaner safety records and equal or better efficacy.
Sarepta Therapeutics (SRPT_) is meeting with U.S. Food and Drug Administration officials this quarter to discuss the possibility of an accelerated approval filing for its DMD drug eteplirsen based on a completed phase II study. Eteplirsen’s adverse event reports have been relatively unblemished to date, with only a single patient reporting transient, non-recurrent proteinuria that did not cause any complications or require treatment to be discontinued.