- |||||||||| budoprutug (TNT119) / Eliem Therap
Enrollment change, Trial withdrawal: Phase 1b/2a in SLE With Budoputug (clinicaltrials.gov) - Oct 16, 2024 P1/2, N=0, Withdrawn, N=40 --> 0 | Not yet recruiting --> Withdrawn
- |||||||||| budoprutug (TNT119) / Eliem Therap
Enrollment closed, Phase classification, Enrollment change, Trial completion date: Efficacy and Safety of VB119 in Subjects With Membranous Nephropathy (clinicaltrials.gov) - Feb 15, 2024 P1/2, N=6, Active, not recruiting, Trial completion date: Aug 2024 --> Oct 2023 | Active, not recruiting --> Terminated; Sponsor change Recruiting --> Active, not recruiting | Phase classification: P1b/2a --> P1/2 | N=30 --> 6 | Trial completion date: Oct 2023 --> Aug 2024
- |||||||||| budoprutug (TNT119) / Eliem Therap
Enrollment closed, Trial completion date, Trial primary completion date: Efficacy and Safety of VB119 in Subjects With Minimal Change Disease (MCD) and Focal Segmental Glomerulosclerosis (FSGS) (clinicaltrials.gov) - Jan 13, 2023 P2, N=20, Active, not recruiting, To date, limited clinical data are available for these investigational treatments and further studies are required to assess their potential value in addressing unmet needs in epilepsy management. Recruiting --> Active, not recruiting | Trial completion date: Feb 2024 --> Nov 2023 | Trial primary completion date: Nov 2023 --> Jun 2023
- |||||||||| KRM-81 / RespireRx, Ztalmy (ganaxolone oral) / Marinus
Review, Journal: The imidazodiazepine, KRM-II-81: An example of a newly emerging generation of GABAkines for neurological and psychiatric disorders. (Pubmed Central) - Mar 9, 2022 These GABAkines and non-steroid compounds (GRX-917, a TSPO binding site ligand), darigabat (CVL-865), an α2/3/5-preferring GABAkine, SAN711, an α3-preferring GABAkine, and the α2/3-preferring GABAkine, KRM-II-81, bring new therapeutic promise to this highly utilized medicinal target in neurology and psychiatry...KRM-II-81 also produces anxiolytic- and antidepressant-like effects in rodent models. Other key features of the pharmacology of this compound are its low sedation rate, lack of tolerance development, and the ability to prevent the development of seizure sensitization.
- |||||||||| ETX-810 / Eliem Therap
Trial completion date, Trial primary completion date: Efficacy and Safety of ETX-018810 in Subjects With Lumbosacral Radicular Pain (clinicaltrials.gov) - Jan 19, 2022 P2, N=122, Recruiting, Other key features of the pharmacology of this compound are its low sedation rate, lack of tolerance development, and the ability to prevent the development of seizure sensitization. Trial completion date: Oct 2021 --> Jul 2022 | Trial primary completion date: Oct 2021 --> Jul 2022
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