Fig. 1: This infographic summarises the design and results of the first phase II trial in Idiopathic Intracranial Hypertension (IIH).
figure 1

The IIH Pressure Trial was a single United Kingdom centre, double-masked, randomised and placebo-controlled trial. It evaluated the use of subcutaneous exenatide, a glucagon-like peptide 1 receptor agonist, and placebo in women with papilloedema secondary to active IIH, with the primary end point at 12 weeks [1]. The trial was a landmark publication as it deployed highly accurate telemetric ICP devices [2]. The intracranial pressure was significantly reduced at all time points in the intervention arm as compared to placebo, independent of weight change.