NEUROLOGICAL DETERIORATION AS A POTENTIAL ALTERNATIVE END-POINT IN HUMAN CLINICAL-TRIALS OF EXPERIMENTAL PHARMACOLOGICAL AGENTS FOR TREATMENT OF SEVERE TRAUMATIC BRAIN INJURIES
Gf. Morris et al., NEUROLOGICAL DETERIORATION AS A POTENTIAL ALTERNATIVE END-POINT IN HUMAN CLINICAL-TRIALS OF EXPERIMENTAL PHARMACOLOGICAL AGENTS FOR TREATMENT OF SEVERE TRAUMATIC BRAIN INJURIES, Neurosurgery, 43(6), 1998, pp. 1369-1372
OBJECTIVE: A recently improved understanding of the pathophysiological
features of head injuries has led to the development of new drug ther
apies. Accurate human clinical trials remain necessary to document the
efficacy and safety of new agents. It would be helpful to decrease th
e time from drug development to clinical use and general availability
for drugs found to be effective. Conversely, ineffective agents could
be abandoned in a timely fashion. RATIONALE: A new endpoint measure, d
efined as neuroworsening (NW), is an objective observable event that i
s identifiable during hospitalization. This may enable the efficacy of
drugs to be demonstrated or disproved much earlier than with 6-month
outcome assessments. The prospective, double-blind, multicenter trial
of the N-methyl-D-aspartate receptor antagonist Selfotel was used to a
cquire data on the efficacy of NW in predicting neurological outcomes.
The 6-month Glasgow Outcome Scale scores, which were the primary endp
oints of that trial, were compared with the frequency of NW. NW was an
observable event that could be objectively defined after head injurie
s. Patients who suffered one or more episodes of NW demonstrated signi
ficantly higher morbidity and mortality rates than did patients who di
d not. CONCLUSION: Future trials should consider the use of NW as an o
utcome measure that can be included with more traditional measures in
the study design. If the strong correlation demonstrated between NW an
d 6-month Glasgow Outcome Scale scores can be prospectively demonstrat
ed in a successful trial, the time to approval of future agents could
be decreased.