scholarly journals 0609 Pharmacokinetics And Formulation Selection Of Ft218, An Investigational Controlled-release Sodium Oxybate Formulation Designed For Once Nightly Dosing

SLEEP ◽  
2019 ◽  
Vol 42 (Supplement_1) ◽  
pp. A242-A243 ◽  
Author(s):  
David Monteith ◽  
Julien Grassot ◽  
Charlotte Castellan ◽  
Thomas Roth
1993 ◽  
Vol 86 (2) ◽  
pp. 208-214 ◽  
Author(s):  
RENÉE J. GOLDBERG ARNOLD ◽  
DIANA J. KANIECKI

Weed Science ◽  
1978 ◽  
Vol 26 (6) ◽  
pp. 679-686 ◽  
Author(s):  
M. M. Schreiber ◽  
B. S. Shasha ◽  
M. A. Ross ◽  
P. L. Orwick ◽  
D. W. Edgecomb

Four starch-encapsulated formulations of EPTC(S-ethyl dipropylthiocarbamate) and of butylate(S-ethyl diisobutylthiocarbamate) were prepared and evaluated by comparison with their respective emulsifiable concentrate formulations for their slow-release capabilities and efficacies. Chemical and biological evaluation indicated that difference in controlled-release could be achieved by the selection of the starch xanthate and oxidant used in the formualtion process. EPTC and butylate released slower when formulated as starch-encapsulated granules than when formulated as emulsifiable concentrates under soil conditions that favored rapid release. The initial release was adequate for weed control and slow enough for desired residual activity. Repeated seeding and harvesting the treated soils and bioassays of treated soils generally produced release rate anticipated from short term dry and wet chemical tests.


2019 ◽  
Vol 64 ◽  
pp. S385
Author(s):  
M. Thorpy ◽  
J. Dubow ◽  
D. Monteith ◽  
J. Grassot ◽  
T. Roth ◽  
...  

SLEEP ◽  
2020 ◽  
Vol 43 (Supplement_1) ◽  
pp. A283-A283
Author(s):  
M Thorpy ◽  
D Seiden ◽  
J Grassot ◽  
D Monteith ◽  
J Dubow ◽  
...  

Abstract Introduction Sodium oxybate is an effective treatment for excessive daytime sleepiness and cataplexy in patients with narcolepsy. The FDA approved formulation requires twice-nightly dosing; at bedtime and 2.5 - 4 hours later. FT218 is a controlled-release formulation of sodium oxybate intended for once-nightly dosing, using Avadel’s proprietary Micropump™ technology. The objective of this study was to evaluate the relative bioavailability of investigational once-nightly sodium oxybate, FT218, 6 g, compared to commercially available twice-nightly sodium oxybate and the food effect of FT218. Methods Two crossover, single-dose pharmacokinetic studies were conducted in healthy volunteers. The first, a relative bioavailability study (n=28) was completed comparing FT218 6 g to twice-nightly sodium oxybate 6 g (in two divided doses of 3 g). The second, evaluated the food effect (n=16) of FT218 6g in the Fed vs. Fasted state. Results FT218 had a lower overall Cmax than twice-nightly sodium oxybate, while AUC was equivalent. C8h level and variability was comparable between FT218 and twice-nightly sodium oxybate. In the Fed, compared to the Fasted state, FT218 had a longer Tmax, lower Cmax and decreased AUC (Cmax 67%, AUC 86%, Tmax 1-hour slower than Fasted values). Adverse Events with FT218 were mostly mild or moderate in severity, non-serious and known AEs associated with sodium oxybate. The safety profiles of FT218 and twice-nightly sodium oxybate at 6 g appeared similar. Conclusion Once-nightly FT218 at 6 g demonstrated a lower overall Cmax and similar exposure to twice-nightly sodium oxybate, with similar C8h plasma levels and C8h variability. In the Fed state, AUC and Cmax of FT218 was lower than in the Fasted State. FT218 was generally safe and well tolerated and the safety profile appeared comparable to twice-nightly sodium oxybate. Support This work was supported by Avadel Pharmaceuticals.


2013 ◽  
Vol 441 (1-2) ◽  
pp. 468-475 ◽  
Author(s):  
Marco Bragagni ◽  
Cristina Beneitez ◽  
Cristina Martín ◽  
Dolores Hernán Pérez de la Ossa ◽  
Paola Angela Mura ◽  
...  

2021 ◽  
Vol 14 (5) ◽  
pp. 442
Author(s):  
Vesela Kostova ◽  
Patrice Désos ◽  
Jérôme-Benoît Starck ◽  
Andras Kotschy

Combining the selective targeting of tumor cells through antigen-directed recognition and potent cell-killing by cytotoxic payloads, antibody-drug conjugates (ADCs) have emerged in recent years as an efficient therapeutic approach for the treatment of various cancers. Besides a number of approved drugs already on the market, there is a formidable follow-up of ADC candidates in clinical development. While selection of the appropriate antibody (A) and drug payload (D) is dictated by the pharmacology of the targeted disease, one has a broader choice of the conjugating linker (C). In the present paper, we review the chemistry of ADCs with a particular emphasis on the medicinal chemistry perspective, focusing on the chemical methods that enable the efficient assembly of the ADC from its three components and the controlled release of the drug payload.


2000 ◽  
Vol 25 (4) ◽  
pp. 402-404 ◽  
Author(s):  
Shigeru TASHIMA ◽  
Shinji SHIMADA ◽  
Motomu NIIKAWA ◽  
Kohei MATSUMOTO ◽  
Reiji TAKEDA ◽  
...  

2015 ◽  
Vol 494 (1) ◽  
pp. 288-295 ◽  
Author(s):  
Marta Casas ◽  
Ángela Aguilar-de-Leyva ◽  
Isidoro Caraballo

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