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Over 1200 families are caring for a loved one with the rare disease ”SynGAP” resulting from a variant of the SYNGAP1 gene. This 10 minute weekly podcast is for them. A quick summary of the latest news in the space. The host is Mike Graglia, co-founder & managing director of the SynGAP Research Fund. SRF is a parent-led, all volunteer public charity in the US that strives to accelerate research into treatments for SYNGAP1 so that we can help our loved ones in a timeframe that matters. Learn more at https://www.syngapresearchfund.org/
Episodes
Thursday Nov 10, 2022
Thursday Nov 10, 2022
ATLANTA: 11/12 https://cbo.io/bidapp/index.php?slug=syngap
Stoke Update on STK-001 Phase 1/2a studies https://investor.stoketherapeutics.com/news-releases/news-release-details/stoke-therapeutics-host-webinar-and-conference-call-present
PMC 11/14-15 https://www.personalizedmedicinecoalition.org/events/Events/Personalized_Medicine_and_the_Patient
188+ Medical Records Matter: Sign up for CIITIZEN: https://www.ciitizen.com/syngap1/
SYNGAP1 ANNUAL MEETING aka “SYNGAP-A-PALOOZA”
NASHVILLE 12/1 & 2 https://secure.givelively.org/event/syngap-research-fund-incorporated/syngap1-conference-2022-charting-our-rare-disease-treatment-path
8-8:30 WELCOME AND BREAKFAST - Lauren
8:30-10:45 SYNGAP1 CAREGIVERS: REALITY, RESILIENCE AND RESOURCES - Becky Sansbury & Nancy Kessler
11:00-12:00 REGISTRIES - Invitae, Simons, Rare-X w/Q&A
12:00-12:30 LUNCH
12:30-1:15 GETTING CLINICAL TRIAL READY - Kathie Bishop, Acadia
1:30-1:55 PRAXIS - Title TBD
1:55-2:40 TAKING ON BEHAVIORS - Jackie Kancir
2:40-3:10 MORE OF EVERYTHING BOOK LAUNCH - JR
3:25-3:50 SRF LATIN AMERICA - FONDO DE INVESTIGATION SYNGAP - Vicky Arteaga
3:50-4:35 SRF YEAR IN REVIEW - Rebecca Kohlhepp, Peter Hallburton, Pavel Gerovich
4:35-5:00 LOOKING TO THE FUTURE - Mike Graglia
6:30-8:30 Community Dinner @ Deacon's New South
JOIN US - 12/1 RECEPTION: https://www.eventbrite.com/e/rare-advocate-reception-tickets-446184007377
JOIN US - 12/2 DINNER:
https://secure.givelively.org/event/syngap-research-fund-incorporated/syngap1-conference-2022-caregiver-dinner
GENETIC THERAPY UPDATES
- #S10e80 https://youtu.be/xeo94GViXiw
- :-) https://www.nytimes.com/2022/11/09/health/pompe-disease-treatment.html
- :-/ http://www.cureffi.org/2022/11/01/asos-hydrocephalus/
- “we are working to develop an ASO against PRNP as a therapy for prion disease…
- Overall, it’s hard to know whether there exists an association between nusinersen and hydrocephalus; if there is, the effect size is not huge and the frequency appears low. No patients appear to have died from it.
- I don’t believe that the tragic results reported for valeriasen should hold us back from bringing a prion disease ASO into trials. But, this is one more reminder that clinical trials are experiments, and the first-in-human dose of a drug is really the starting line and not the finish line.”
SMA: THREE DRUGS! BIG Pipeline. https://www.curesma.org/sma-drug-pipeline/
Angelman Trials: 3 recruiting. https://clinicaltrials.gov/ct2/results?cond=Angelman+Syndrome&term=&cntry=&state=&city=&dist=
Dravet Trails, 7 recruiting, 1 is ASO with Stoke. https://clinicaltrials.gov/ct2/results?cond=Dravet+Syndrome&Search=Apply&recrs=a&age_v=&gndr=&type=&rslt=
CANNONBALL 2.0 - $156,802 Listen to the Radio interview! https://www.syngapresearchfund.org/cannonball
This is a podcast: subscribe to and rate this 10 minute #podcast #SYNGAP10 here https://www.syngapresearchfund.org/syngap10-podcast
Apple podcasts: https://syngap.fund/10a
Episode 80 of Syngap10 - November 10, 2022
#Syngap #SYNGAP1 #epilepsy #autism #intellectualdisability #id #anxiety #raredisease #epilepsyawareness #autismawareness #rarediseaseresearch #SynGAPResearchFund #CareAboutRare #PatientAdvocacy #GCchat #Neurology
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