A prospective, double-blind, randomized study of high-versus low-dose OKT3 induction immunosuppression in cadaveric renal transplantation

1994 ◽  
Vol 7 (5) ◽  
pp. 356-361 ◽  
Author(s):  
Douglas J. Norman ◽  
Jess A. Kimball ◽  
William M. Bennett ◽  
Fuad Shihab ◽  
Thomas D. Batiuk ◽  
...  
1994 ◽  
Vol 7 (5) ◽  
pp. 356-361
Author(s):  
Douglas J. Norman ◽  
Jess A. Kimball ◽  
William M. Bennett ◽  
Fuad Shihab ◽  
Thomas D. Batiuk ◽  
...  

2020 ◽  
pp. 108705472090908 ◽  
Author(s):  
Gianpiera Ceresoli-Borroni ◽  
Azmi Nasser ◽  
Toyin Adewole ◽  
Tesfaye Liranso ◽  
Jiahong Xu ◽  
...  

Objective: To evaluate efficacy and safety of SPN-810 (extended-release molindone) in a Phase-2b, randomized, double-blind, placebo-controlled, dose-ranging study of children (6–12 years) with ADHD and persistent impulsive aggression (IA). Method: After lead-in, children were randomized to (a) placebo ( N = 31); (b) low-dose ( N = 29, 12/18 mg/day); (c) medium-dose ( N = 30, 24/36 mg/day); and (4) high-dose ( N = 31, 36/54 mg/day) groups. Treatment included ~2.5-week titration, 3-week maintenance, and 1-week tapering/conversion, alongside existing monotherapy (stimulants/nonstimulants) and behavioral therapy. The primary endpoint was change in Retrospective-Modified Overt Aggression Scale (R-MOAS) score at end of study, with safety monitored. Results: A total of 95 (78.5%) children completed the study. Aggression (R-MOAS) improved with low and medium doses (low dose: p = .031; medium dose: p = .024; high dose: p = .740). The most common adverse events were headache (10.0%), sedation (8.9%), and increased appetite (7.8%). Conclusion: These results suggest SPN-810 may be effective in reducing residual IA behaviors in children with ADHD. Research is still needed to support the benefit–risk profile of SPN-810 in pediatric populations.


1984 ◽  
Vol 37 (4) ◽  
pp. 373-377 ◽  
Author(s):  
A. J. F. DCARAPICE ◽  
G. J. BECKER ◽  
P. KINCAID-SMITH ◽  
T. H. MATHEW ◽  
J. NG ◽  
...  

1983 ◽  
Vol 61 (20) ◽  
pp. 991-1000 ◽  
Author(s):  
G. Thiel ◽  
F. Harder ◽  
R. L�rtscher ◽  
M. Br�nisholz ◽  
J. Landmann ◽  
...  

1988 ◽  
Vol 45 (2) ◽  
pp. 320-322 ◽  
Author(s):  
Ben A. Vanderwerf ◽  
Arnold I. Serota

1996 ◽  
Vol 7 (5) ◽  
pp. 792-797
Author(s):  
C Ponticelli ◽  
G Civati ◽  
A Tarantino ◽  
F Quarto di Palo ◽  
G Corbetta ◽  
...  

This study presents the 10-yr follow-up results of a multicenter controlled trial on 108 recipients of cadaveric renal transplantation, randomized to receive cyclosporine (N = 55) or azathioprine (N = 53), both in combination with steroids. The 10-yr patient survival rate was 89% in the cyclosporine group and 83% in the azathioprine group (P = not significant [NS]); the 10-yr graft survival was 56% and 35%, respectively (log-rank test, P = 0.009). The half-life of grafts functioning after 1 yr was 15.4 +/- 3.9 versus 10.6 +/- 3.6, P = NS). The rate of early rejection in the cyclosporine group was significantly lower than that in the azathioprine group (0.30 versus 1.4, P < 0.01). Although the mean creatinine clearance rate was always higher in the azathioprine group, the decline in graft function from the first to the tenth yr was not significantly different between the two groups (-13.0 +/- 16.4 versus -12.3 +/- 19 mL/min, P = NS). In cadaveric renal transplantation, cyclosporine allows better graft survival than azathioprine, not only in the short term but also in the long term, with similar attrition of graft function for up to 10 yr.


Oncotarget ◽  
2016 ◽  
Vol 7 (11) ◽  
pp. 12089-12101 ◽  
Author(s):  
Guang-hui Pan ◽  
Zheng Chen ◽  
Lu Xu ◽  
Jing-hui Zhu ◽  
Peng Xiang ◽  
...  

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