Lanoteplase is a recombinant plasminogen activator, which when administered
as a single bolus intravenous injection, displays thrombolytic activity.
In the phase II InTIME trial, lanoteplase dose-dependently increased reperf
usion rates at 60 and 90 minutes in patients with acute myocardial infarcti
on and at 90 (but not 60) minutes lanoteplase 120 kU/kg was significantly s
uperior to alteplase in restoring TIMI grade 2 and 3 flow (in 83.0 and 71.4
% of patients, respectively).
Preliminary results from the phase III InTIME-II study showed that lanotepl
ase was as effective as alteplase in decreasing 30-day mortality.
At 30 days, the combined incidence of death, reinfarction, major bleeding a
nd heart failure was lower with lanoteplase 120 kU/kg than with alteplase 1
00mg.
From preliminary results of the large InTIME-II study, lanoteplase 120 kU/k
g showed a greater incidence of intracranial haemorrhage and mild bleeding
than alteplase less than or equal to 100mg, but a similar incidence of stro
ke. The smaller InTIME study showed a tendency for fewer adverse events wit
h lanoteplase.