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Actelion's brain haemorrhage drug clazosentan fails to meet endpoint in CONSCIOUS-2 study

Basel, SwitzerlandThursday, September 30, 2010, 08:00 Hrs  [IST]

Actelion Ltd announced the initial results of CONSCIOUS-2 a clinical study evaluating the safety and efficacy of clazosentan in reducing vasospasm-related morbidity and all-cause mortality in clipped patients following aneurysmal subarachnoid haemorrhage (aSAH). The primary endpoint showed a non-significant relative risk reduction of 17 percent in favour of clazosentan (p=0.1). The safety profile of clazosentan in CONSCIOUS-2 was comparable to previous studies with the compound in this disease. Jean-Paul Clozel, MD and chief executive officer of Actelion commented: "These are, of course, disappointing results. Having embarked upon such a complex study, both in terms of design and execution, I must commend the exceptional efforts of all involved delivering a high-quality study." Jean-Paul Clozel continued: "Actelion will continue to focus on growing its existing business. With four marketed products, Actelion is generating the necessary revenues to continue to invest appropriately in clinical studies for our more than 10 development compounds." In regards to the ongoing CONSCIOUS-3 study in patients with aSAH that underwent coiling to secure their aneurysm, Actelion will discuss the appropriate course of action with the Steering Committee. The company will provide an update on the clazosentan development programme in its upcoming Q3 reporting, scheduled for Thursday, 21 October 2010. CONSCIOUS-2 (Clazosentan to Overcome Neurological iSChemia and Infarct OccUrring after Subarachnoid haemorrhage) investigated the potential clinical benefits of clazosentan through the primary endpoint of vasospasm-related morbidity and all-cause mortality, which includes neurological deterioration, new brain infarcts, introduction of vasospasm rescue therapy, or death from any cause. CONSCIOUS-2 was a global study which concluded enrolment with over 1,150 patients with aSAH and aneurysmal surgical clipping, from more than 100 centres. Patients were randomized 2:1 to receive either 5 mg/h of clazosentan, or placebo. Aneurysmal subarachnoid haemorrhage (aSAH) is a life-threatening condition affecting over 85,000 people in the EU, US and Japan every year. This condition occurs when the rupture of an aneurysm on the cerebral vessels leads to release of blood into the subarachnoid space of the brain. Endovascular coiling or microsurgical clipping is usually required to stop the bleeding and prevent further episodes. Cerebral vasospasm following SAH causes the intracranial arteries to constrict thus diminishing blood flow to the brain. It is a significant predictor of poor outcome and the leading potentially treatable cause of mortality and morbidity in these patients. Vasospasm is unpredictable in nature and seen in over 67 per cent of untreated patients with angiography at the time of maximum spasm, around the end of the first week. It becomes symptomatic in about half of these patients. Currently, there is no effective treatment for the prevention and treatment of the severe complications following vasospasm. CONSCIOUS-3 is a phase III study evaluating the efficacy and safety of two doses (5 or 15 mg/h) of clazosentan versus placebo in patients post-aSAH treated by endovascular coiling. The primary endpoint is identical to that of CONSCIOUS 2. Until the end of September 2010, the study enrolled close to 600 patients out of 1500 planned. CONSCIOUS-1 was a multi-centre, international, double-blind, randomized, placebo-controlled, parallel-group, dose-finding study to evaluate the efficacy of three dose levels of clazosentan (15, 5 and 1mg/hour) in preventing the occurrence of cerebral vasospasm following aSAH in patients who underwent either clipping or coiling to stop the initial bleed, assessed by angiography. CONSCIOUS-1 showed a strong treatment effect on the primary endpoint. Clazosentan significantly reduced moderate/severe vasospasm at all tested doses, with a relative risk reduction compared to placebo of 65 per cent at the highest dose. A post-hoc analysis showed a trend in favour of reducing morbidity/mortality related to vasospasm using central assessment. In the study, treatment with clazosentan was associated with more adverse events than placebo, mainly related to vasodilatory effects such as hypotension and fluid retention. Actelion Ltd is a biopharmaceutical company with its corporate headquarters in Allschwil/Basel, Switzerland. Actelion's first drug Tracleer, an orally available dual endothelin receptor antagonist, has been approved as a therapy for pulmonary arterial hypertension.

 
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