Consensus could be reached that there is overwhelming evidence of preclinic
al neuroprotection. However, the evidence of neuroprotection/neurorescue un
der clinical conditions is limited. Lessons from clinical trials designed t
o show neuroprotection (selegiline, amantadine, dopamine agonists) demonstr
ate that with the drugs available neuroprotection/neurorescue has to start
as early as possible. A PET-controlled clinical trial with ropinirole shows
that there seems to be a good chance for neuroprotection in the early phas
e of Parkinson's disease in patients treated from the very beginning of the
disease while there is no such benefit in patients with a late start of a
neuroprotective therapeutic strategy. Also long-term neuroprotection cannot
be reached. Complicating factors to demonstrate clinical neuroprotection a
re discussed.