pd 98059 has been researched along with Abnormalities, Multiple in 1 studies
2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one: inhibits MAP kinase kinase (MEK) activity, p42 MAPK and p44 MAPK; structure in first source
2-(2-amino-3-methoxyphenyl)chromen-4-one : A member of the class of monomethoxyflavones that is 3'-methoxyflavone bearing an additional amino substituent at position 2'.
Abnormalities, Multiple: Congenital abnormalities that affect more than one organ or body structure.
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Chang, JG | 1 |
Hsieh-Li, HM | 1 |
Jong, YJ | 1 |
Wang, NM | 1 |
Tsai, CH | 1 |
Li, H | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
In Vivo Study of Safety, Tolerability and Dosing Effect on SMN mRNA and Protein Levels of Valproic Acid in Patients With Spinal Muscular Atrophy[NCT00374075] | Phase 1 | 42 participants | Interventional | 2003-09-30 | Completed | ||
Phase I/II Trial of Valproic Acid and Carnitine in Infants With Spinal Muscular Atrophy Type I (CARNI-VAL Type I)[NCT00661453] | Phase 1/Phase 2 | 40 participants (Actual) | Interventional | 2008-04-30 | Completed | ||
Multi-center Phase II Trial of Valproic Acid and Carnitine in Patients With Spinal Muscular Atrophy (SMA CARNI-VAL Trial)[NCT00227266] | Phase 2 | 94 participants (Actual) | Interventional | 2005-09-30 | Completed | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
(NCT00661453)
Timeframe: -2 weeks, time 0, 3 months, 6 months
Intervention | g (Mean) | |||||
---|---|---|---|---|---|---|
Lean Mass Baseline | Lean Mass 3 months | Lean Mass 6 months | Fat Mass Baseline | Fat Mass 3 months | Fat Mass 6 months | |
SMA Type 1 | 4317.15 | 4993.92 | 5133.83 | 3011.37 | 3618.25 | 4316.08 |
The maximum Compound Motor Action Potential (CMAP) is a measurement obtained through EMG testing that is associated with disease progression. In this study, we measure the maximum CMAP by stimulating one nerve in the hand and measuring the response of the muscle. This is done multiple times, the outcome used is the highest peak, or response observed. (NCT00227266)
Timeframe: 1 month prior to official enrollment, beginning of study (0 months), 6 months, 12 months (data point not available)
Intervention | mV (Mean) | |
---|---|---|
Baseline | 6 months | |
Cohort 1a Sitters Placebo Then Treatment | 2.28 | 2.32 |
Cohort 1b Sitters Treatment | 2.93 | 2.37 |
Cohort 2 Standers and Walkers - Treatment | 5.52 | 6.56 |
The maximum Compound Motor Action Potential (CMAP) is a measurement obtained through EMG testing that is associated with disease progression. In this study, we measure the maximum CMAP by stimulating one nerve in the hand and measuring the response of the muscle. This is done multiple times, the outcome used is the highest peak, or response observed. (NCT00227266)
Timeframe: 1 month prior to official enrollment, beginning of study (0 months), 6 months, 12 months (data point not available)
Intervention | mV (Median) | |
---|---|---|
Baseline | 6 months | |
Cohort 1a Sitters Placebo Then Treatment | 1.91 | 1.44 |
Cohort 1b Sitters Treatment | 2.2 | 1.8 |
Cohort 2 Standers and Walkers - Treatment | 5.3 | 5.85 |
The maximum Compound Motor Action Potential (CMAP) area is a measurement obtained through EMG testing that is associated with disease progression. In this study, we measure the maximum CMAP by stimulating one nerve in the hand and measuring the response of the muscle. This procedure is repeated multiple times. The maximum area is the response that results in the largest area under the response curve. (NCT00227266)
Timeframe: 1 month prior to official enrollment, beginning of study (0 months), 6 months, 12 months (data point not available)
Intervention | mVms (Mean) | |
---|---|---|
Baseline | 6 months | |
Cohort 1a Sitters Placebo Then Treatment | 5.46 | 5.28 |
Cohort 1b Sitters Treatment | 5.45 | 5.26 |
Cohort 2 Standers and Walkers - Treatment | 14.85 | 16.26 |
The maximum Compound Motor Action Potential (CMAP) area is a measurement obtained through EMG testing that is associated with disease progression. In this study, we measure the maximum CMAP by stimulating one nerve in the hand and measuring the response of the muscle. This procedure is repeated multiple times. The maximum area is the response that results in the largest area under the response curve. (NCT00227266)
Timeframe: 1 month prior to official enrollment, beginning of study (0 months), 6 months, 12 months (data point not available)
Intervention | mVms (Median) | |
---|---|---|
Baseline | 6 months | |
Cohort 1a Sitters Placebo Then Treatment | 3.6 | 3.74 |
Cohort 1b Sitters Treatment | 4.6 | 3.4 |
Cohort 2 Standers and Walkers - Treatment | 13.65 | 16.85 |
Comparison of Modified Hammersmith Change from baseline to 6 months. Scores range from 0 to 40. A higher score indicates a better outcome. This scale is used to assess gross motor abilities of non-ambulant children with SMA in multiple research trials as well as in clinical settings. (NCT00227266)
Timeframe: 0 months, 6 months
Intervention | Score (Mean) | ||
---|---|---|---|
Baseline visit (0 weeks) | 6 Month visit (V2) | Change from Baseline | |
Cohort 1a Sitters Placebo Then Treatment | 20.0 | 20.6 | 0.6 |
Cohort 1b Sitters Treatment | 16.6 | 16.8 | 0.2 |
"Baseline Modified Hammersmith Extend testing. The baseline test is the score they receive during their screening visits. This scale ranges from 0 to 56. A higher score indicates a better outcome.~This scale is used to assess gross motor abilities of children with SMA in multiple research trials as well as in clinical settings." (NCT00227266)
Timeframe: 1 month prior to enrollment, at enrollment (0 months)
Intervention | Score (Mean) | |
---|---|---|
Modified Hammersmith Extend at S1 (-4 weeks) | Modified Hammersmith Extend at S2 (0 weeks) | |
Cohort 2 Experimental | 47.0 | 48.3 |
1 other study available for pd 98059 and Abnormalities, Multiple
Article | Year |
---|---|
Treatment of spinal muscular atrophy by sodium butyrate.
Topics: Abnormalities, Multiple; Alternative Splicing; Animals; Butyrates; Cell Line, Transformed; Crosses, | 2001 |
Treatment of spinal muscular atrophy by sodium butyrate.
Topics: Abnormalities, Multiple; Alternative Splicing; Animals; Butyrates; Cell Line, Transformed; Crosses, | 2001 |
Treatment of spinal muscular atrophy by sodium butyrate.
Topics: Abnormalities, Multiple; Alternative Splicing; Animals; Butyrates; Cell Line, Transformed; Crosses, | 2001 |
Treatment of spinal muscular atrophy by sodium butyrate.
Topics: Abnormalities, Multiple; Alternative Splicing; Animals; Butyrates; Cell Line, Transformed; Crosses, | 2001 |
Treatment of spinal muscular atrophy by sodium butyrate.
Topics: Abnormalities, Multiple; Alternative Splicing; Animals; Butyrates; Cell Line, Transformed; Crosses, | 2001 |
Treatment of spinal muscular atrophy by sodium butyrate.
Topics: Abnormalities, Multiple; Alternative Splicing; Animals; Butyrates; Cell Line, Transformed; Crosses, | 2001 |
Treatment of spinal muscular atrophy by sodium butyrate.
Topics: Abnormalities, Multiple; Alternative Splicing; Animals; Butyrates; Cell Line, Transformed; Crosses, | 2001 |
Treatment of spinal muscular atrophy by sodium butyrate.
Topics: Abnormalities, Multiple; Alternative Splicing; Animals; Butyrates; Cell Line, Transformed; Crosses, | 2001 |
Treatment of spinal muscular atrophy by sodium butyrate.
Topics: Abnormalities, Multiple; Alternative Splicing; Animals; Butyrates; Cell Line, Transformed; Crosses, | 2001 |