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CURE SYNGAP1 PODCAST aka SYNGAP10

CURE SYNGAP1 PODCAST aka SYNGAP10

Business:Non-Profit

The Coast 2 Coast Challenge benefiting the SYNGAP1 #ProMMiS for Clinical Excellence is critical. #S10e152

The Coast 2 Coast Challenge benefiting the SYNGAP1 #ProMMiS for Clinical Excellence is critical. #S10e152

2024-10-22
Download

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?
    • Replicable/scalable required by regulators
    • Accessibility (not primary reason)
    • Establish more locations where trials will be managed
    • Laying a foundation for a national self-sustaining network
    • 3 is the minimum, look at STARR or Angelman, both had/ve 4.
  • 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: 

https://Syngap.Fund/West & https://Syngap.Fund/East

view more

More Episodes

We need to raise funds for the critical work of CURE SYNGAP1, join us with #Sprint4SYNGAP #S10e201
2026-03-06 62
#RareDiseaseWeek! We are doing much beyond grants… too much. Get the Citizen Health App! #S10e200
2026-02-25 86
Support Clinical Trial Design for #SYNGAP1 via biobanks, EEGs and Fundraising. #S10e199
2026-02-17 77
All #SYNGAP1 Families need to take part in our Natural History Studies: ProMMiS & Citizen #S10e198
2026-02-06 91
Funding Priorities. Biorepository. Genetic Testing. How to move for a clinical trail! #S10e197 Monday, February 2, 2026 - Week 6
2026-02-02 72
Stoke Tx shows us that ASO Clinical Development is accelerating. #S10e196
2026-01-16 85
SYNGAP1 Related Disorder (SRD) Key Talking Points & why we need to use them. #S10e195
2026-01-11 84
Becky Quick launches CNBC Cures, Finding Your Voice & Key Talking Points for SRD! #S10e194
2026-01-09 103
Stockdale Paradox: Not getting out at Xmas, but we will win. #SynGAPCensus = 1,707. #S10e193
2026-01-02 86
AES ‘25 was incredible, Fundraising, PRV, Behaviors, Posters/Pubmed & Thank you. #S10e192
2025-12-20 86
New book by #SYNGAP1 mom for and about #GlassChild (Sibling of Special Needs) #S10e191
2025-12-01 99
AAV. Resources on cureSYNGAP1.org. Congrats to Ultragenyx & Novartis. Conf is in 5 days! #S10e190
2025-11-27 83
#CureSYNGAP1 Conf: 1 week! #GivingTuesday: 5 days. #ProMMiS. Mvmt & Sleep papers. #S10e189
2025-11-27 68
It’s time to UNLOCK THEIR TOMORROW - let’s raise funds. Also: CAMP4 and our name. #S10e188
2025-11-09 80
Clinical Research, AI Dx, #NL47, Survey, #Autism Press, 6 Days to Register for #SYNGAP1conf #S10e187
2025-10-25 80
#SyngapCenus 1,675 Teacher Handout CC/VNS Citizen Paper $CAMP starts GLP Tox CIRM funds S1 #S10e186
2025-10-03 95
F78.A1,the code for #SYNGAP1, turns 4, make sure we use it. #ICD10 for #RareDisease Update. #S10e185
2025-09-30 77
DSC - RDCRN - NCATS - NIH Press! #AAV in #Cell. SRF at CB. Scramble for SYNGAP1 next week! #S10e184
2025-09-26 76
You need a #CRID. SRF $1M to $CAMP noticed in Equity Research! #BeaconOfHope was great. #S10e183
2025-09-26 70
CURE SYNGAP1 joins biotech investors in CAMP4 Tx’s $100M Raise for ASO Program $CAMP #S10e182
2025-09-10 114
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