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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
Tuesday Oct 22, 2024
Tuesday Oct 22, 2024
Tuesday, October 22, 2024
First Principles
- Genetic disease means that gene broken since conception.
- Novel medicines are possible ways to fix the gene - Genetic Therapies (ASO &/or AAV), this is recent, before now, kids with these diseases were a “go home and love them” situation.
- These are delivered via spinal tap or directly to the brain in leading medical centers.
- First though, regulators must approve.
Our job
- Develop medicines or get industry to - This is happening see Pipeline
- Get regulators to approve trials
- Get medical centers up to speed on SYNGAP1-Related Disorders (SRD)
What we are building on
- CHOP ENDD funded externally (see #S10e92) and replicating what was built for STXBP1, check last week’s webinar https://curesyngap1.org/resources/webinars/93-endd-chop-2024-syngap1/
- Rare-X platform for PRO collection
- Regulatory pathway being made clearer every day by Stoke (Dravet), Praxis (SCN2A), Ionis (many) all of whom are working on SYNGAP1 as well.
What we are asking for
- We need to raise at least $500k (3rd site), preferably $1.13M (ProMMiS)
- Make your largest gift ever to SRF
- Fundraise with friends and family
- ACES is now ProMMiS, who knew ACE meant Adverse Childhood Event, not us.
Key slides: S1 Path to Treatment | 2024 (09.27.24)
- 1. Why Now? Why is it time to go from bench to bedside (research to clinical)?
- At least 10 companies on our pipeline not to mention multiple small molecule efforts
- We have limited resources – so the focus has to transition, clinical funding first.
- CHOP Gift is 1 year down…
- 2. Why NHS?
- Understand SYNGAP1 better, go beyond Vlaskamp 2019 and Wiltrout 2024, see #S10e105
- FYI at CHOP, as I shared in #S10e151, at year 1, we are at – 86 (Visits) + 10 (new scheduled) + 19 (2nd) + 4 (3rd) + 22 (follow up)
- Learn what to measure in clinical trials for SRD, remember our seizures are challenging
- Ideally we develop a Synthetic Control Arm if we use GCP
- Why top shelf? We need institutions the FDA will take seriously and our children are very complex requiring experienced clinicians.
- 3. Why Multidisciplinary.
- Neuro, Psych, Genetics, PT, ST, OT, GI, Sleep, ENT, Ortho.
- Beyond the sheer burden of getting our kids out and about for multiple appointments the coordination by a parent is almost impossible.
- 4. Why Multisite/3 sites?
- 5. How and why so fast?
- Because we can. Time is Brain.
- Following a well trodden path
- SMA, Rett, Angelman, Dravet, but we are moving FASTER.
- 6. Does the industry really care?
- We are next there are so so many behind us, eager to take the resources we have access to today.
- Market size (Per our Census 425 US/1500 global is tip of iceberg)
- Multiple players reassuring each other
- Relatively strong amount of scientific and clinical research
- Haploinsufficiency (like Dravet – STOKE) – so relatively easy
- 7. Expensive?
- No. Clinical Research is more expensive than basic scientific research.
- Leveraging CHOP and Rare-X, setting up required networks to prepare for clinical trials.
- It’s time.
- 8. Why Bother/Help?
- Now is the time for SYNGAP1, we miss it at our peril.
- Sure, once in these places we will still see our patients, but the study, the support and the focus may pass.
- Our kids don’t die, regardless of patient age, what we are doing can change their future and that of their loved ones and caregivers.
- If not us, then who? It is a rare exception when a non-family member gives a gift, and it is always because a family member asked. We must ask.
- 9. What can I do?
- Donate to, share, join our Coast2Coast Clinics Challenge – two SYNGAP1 Squads in West and East – it’s critical
- $500k goal by end of 2024; more than $1M needed just for the SYNGAP1ProMMiS. So far, donations from $25 to $25,000 – each and every contribution matters.
- This requires our entire S1 network to solicit family, friends, work colleagues, companies, etc. to contribute. Many causes out there – why not ours?
- Syngap.Fund/C2C
https://Syngap.Fund/C2C > https://secure.givelively.org/donate/syngap-research-fund-incorporated/coast2coast-clinics-challenge
Two teams:
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