Page last updated: 2024-10-15

d-jnki-1

Description

D-JNKI-1: a synthetic, cell permeable peptide that blocks the MAPK-JNK signal pathway; has potential therapeutic value for long-term protection of both the morphological integrity and physiological function of the organ of Corti during times of oxidative stress [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID156963743
MeSH IDM0455086

Synonyms (1)

Synonym
d-jnki-1

Toxicity

ExcerptReference
" Safety was evaluated by the frequency of clinically relevant hearing deterioration and adverse events."( Efficacy and safety of AM-111 in the treatment of acute sensorineural hearing loss: a double-blind, randomized, placebo-controlled phase II study.
Bodlaj, R; Domka, W; Kabacinska, A; Klimak, P; Kostrica, R; Lisowska, G; Meyer, T; Morawski, K; Suckfuell, M, 2014
)
" Patients were evaluated at 24, 48 h, 8, and 28 days following the administration of XG-102, including laboratory tests, standard eye examinations, vital signs, and occurrence of adverse events."( Subconjunctival injection of XG-102, a JNK inhibitor peptide, in patients with intraocular inflammation: a safety and tolerability study.
Behar-Cohen, F; Beydoun, T; Combette, JM; Deloche, C; Kirwan, BA; Perino, J, 2015
)
"A total of 17 non-serious adverse events, considered unrelated to the study treatment, were reported for 10 patients."( Subconjunctival injection of XG-102, a JNK inhibitor peptide, in patients with intraocular inflammation: a safety and tolerability study.
Behar-Cohen, F; Beydoun, T; Combette, JM; Deloche, C; Kirwan, BA; Perino, J, 2015
)
"In this first clinical trial using XG-102, administered as a single subconjunctival injection as adjunct therapy, in patients with recent post-surgery or post-trauma intraocular inflammation is safe and well tolerated."( Subconjunctival injection of XG-102, a JNK inhibitor peptide, in patients with intraocular inflammation: a safety and tolerability study.
Behar-Cohen, F; Beydoun, T; Combette, JM; Deloche, C; Kirwan, BA; Perino, J, 2015
)
" Safety was evaluated by the frequency of clinically relevant hearing deterioration and adverse events."( Efficacy and Safety of AM-111 in the Treatment of Acute Unilateral Sudden Deafness-A Double-blind, Randomized, Placebo-controlled Phase 3 Study.
Jokovic, G; Karpishchenko, S; Kienle-Gogolok, A; Krzyzaniak, A; Lin, CD; Meyer, T; Navratil, P; Staecker, H; Tzvetkov, V; Wright, N, 2019
)
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (57)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's23 (40.35)29.6817
2010's34 (59.65)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials5 (8.62%)5.53%
Reviews5 (8.62%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other48 (82.76%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]