Oct 5 2012
MannKind Corporation (Nasdaq: MNKD) today announced that it has
completed recruiting patients for two Phase 3 clinical studies of AFREZZA®
(insulin human [rDNA origin]), an investigational, ultra rapid-acting
mealtime insulin therapy, administered using MannKind's to-be-marketed
next-generation inhaler.
The first of these studies (study 171) is an open-label study in
patients with type 1 diabetes. After a run-in period, during which all
patients are optimized on their basal insulin regimen, at least 471
subjects are to be randomized to one of three arms for mealtime insulin:
a control arm, in which patients utilize injected rapid-acting insulin,
or one of two AFREZZA arms, one for the MedTone inhaler and the other
for the next-generation inhaler. After the mealtime insulin is titrated,
there is a 12-week observation period on stable doses of the mealtime
insulin to assess HbA1c levels, which is the primary outcome parameter.
Another objective of this study is to compare the safety profile of the
two AFREZZA treatment groups.
The other study (study 175) is assessing AFREZZA using the
next-generation inhaler in patients with type 2 diabetes whose disease
is inadequately controlled on metformin with or without a second or
third oral medication. After a run-in period during which the subjects
remain on their oral medication, at least 328 patients will be
randomized to additional treatment with AFREZZA or to Technosphere®
inhalation powder (placebo). The study will also have a titration
period, followed by a 12-week evaluation period to assess HbA1c levels.
"Completing patient recruitment is the initial element, and often the
lengthiest, in the conduct of large scale Phase 3 clinical trials," said
Alfred Mann, Chairman and Chief Executive Officer. "Both studies are on
track to be completed in the second quarter of 2013 and we expect to
report top-line results next summer. Our objective is to resubmit the
NDA for AFREZZA in the third quarter of next year."
Source: MannKind Corporation