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TDP-43 self-interaction is modulated by redox-active compounds Auranofin, Chelerythrine and Riluzole

~380-hour half-life supports extended dosing interval

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All earlier GHRPs including GHRP-2 and GHRP-6 stimulated GH release but also produced dose-dependent elevations in ACTH and cortisol through activation of broader stress-response signalling pathways

Conversely, patients who did not respond well to high-dose IFN- 1a monotherapy seemed to benefit more from low-dose atorvastatin (280)