Scenario / Disease-Model Questions, Safety De-Risking Strategy, Sharefolder, Parkin Protein Notes, And Assays Table

Scenario의 개념 (least robust – most robust)Is disease model necessary?
- 정상인의 brain parkin protein level 이 A (Soon NSTM will define this) 라면,
- NHP 연구를 통해, 이것을 달성시키는 Dose B를 define 히면 이것이 그냥 HED 아닌가?
Dose B를 nhp 에 주었을 때의 CSF parkin level 이 C 라면, 임상에서 csf C 로 확인하면 되지 않나?
Disease model 은 neuroprotection과 연결시켜서 노랑을 strengthen 시킬 수 있을 것.
Is a PD marker necessary?(특히 disease model이 없다면), PD change 로 노랑을 strengthen 시킬 수 있을 것.
NHP 1M BD studyHow many doses?

Safety

MOAFrequencyConsequenceIn vitrotranslatabilityDe-risking strategy (preclinical)
In vivo / translatability
BMRoute?Monitorable?Clinic Manageable?BM
GT-generalimunogenecityCapsidCommon↓ efficacy,
↑ cytotoxicity
Should be evident in vivo studies
Unclear
?
transgeneCommonEfficacy, safety (cytotoxicity)In vivo studies
unclear
DRG degenerationUPR → inflammation → cytotoxicityCapsid/transgeneNot common (almost universal in NHP)Cytotoxicity (DRG)UPR gene expression analysisUPR gene expression analysisNeurosurgery
Parkin-specific↑ DA neuronal loss in SNTransgeneCheck the effect in DA neurons (pharmacology)
Histopathology of brain in relatively long-term (3 months or more) NHP biodistribution and tox studies
NeurosurgeryJs; DATScan?Js: not manageable
↑ mt density in muscletransgeneNeurosurgery
Muscle hypertrophytransgenemiddleHistopathology of skeletal muscles in NHP biodistribution and toxicology studiesNeurosurgeryJs: m biopsy?Js: manageable (recoveralbe)
Parkin-specific↑ fibrosis in heart
↑ Parkin → ↑ calcium dysregulation → cardiac hypertrophy
transgenemiddleHistopathology of heart and lung in NHP biodistribution and toxicology studies
ECG/Echo in biodistribution and exploratory toxicity study
ECG/Echo 겠네NeurosurgeryJs: ECG/EchoJs: manageable (recoverable)ECG/Echo 겠네
T-generalGenotoxicity (unwanted insertion of transgene DNA into host chromosome)Not commontumorFDA is no longer concerned.

Sharefolder

  • Mouse poc study 에서 BM? → DMPK 와 논의하자
  • 내 생각: MC1 ARG IN MICE POC study or NHP BD study?

[https://mytakeda.sharepoint.com/sites/InterACT-RAD-Pipeline/Parkin%20Gene%20Therapy/Shared%20Documents/Forms/AllItems.aspx?RootFolder=%2Fsites%2FInterACT%2DRAD%2DPipeline...]

[https://mytakeda.sharepoint.com/sites/InterACT-RAD-Pipeline/Parkin%20Gene%20Therapy/Shared%20Documents/Forms/AllItems.aspx?RootFolder=%2Fsites%2FInterACT-RAD-Pipeline%2FParkin%20Gene%20Therapy%2FShared%20Documents%2FMeeting%20Minutes%20and%20Materials&FolderCTID=0x0120007803EDB3EB43F94B88445EA2823B1719&View=%7B1B1D5A2D%2D5E8C%2D41AB%2D978F%2D618DC69212AC%7D]

Timeline

[Parkin GT Scenarios and Timelines.pptx]

Resources: my PGRN in this document

  • Parkin protein:
    • Parkin KO mice
    • Sensitivity, linearity, stability, selectivity
    • Human pooled CSF → PD Patient CSF
    • Check cross-reactivity to mouse parkin (although we will need to measure only human parkin)
      • MPTP study에서는, mice parkin 이 많이 있으므로 구분해야 할 것.
        • How?

Option 1. Mouse Brain homogenate에서 detectability 확인 (이거라 함) Option 2. 위 과정 없이 바로 CSF 측정 Option 3. Mouse CSF 에서 detectability 확인 (right after we confirm detectability in human CSF)

  • How long does it take?

  • Questions

    • Who analysis brain pS65Ub?
    • Can we freeze mouse CSF and measure when our assays are ready?
      • May be feasible, caveat is that we don’t normaly test longterm stability
    • What does it take for the assay to be ready for mouse studies?
    • Parkin BM timeline 등 자세히 없으니 만들자
    • Confidence 측면에서) asset generation timeline 과 맞춘다
    • Resource prioritization 필요함.

Assays

AssayBuffer LLOQConcentration noteNBB result-CSFCSFRequired volume
Parkin0.061 pg/mL10 times concentration from 1 mL n 7
Minimum 0.7
Maximum 2.500
NBB sample
For 1ml, 1.3/0.061 pg/ml = 21x (this is window),
For 500ul LLOQ is 0.12 pg/ml, so then window is only 11x.
1.5 mL 이라는데?

Uncertain Spans

locationtranscriptionuncertainty
Safety table column structurethe wide multi-column header / sub-header arrangementThe De-risking strategy block visually splits into “preclinical” (In vivo / translatability / BM) and “Clinic” (Route? / Monitorable? / Manageable? / BM) groupings; column boundaries between these groups are best read from the body_full and derisking_table evidence images.
Sharefolder URL #1trailing path is wrapped and truncated by the photo edgeThe first SharePoint URL ends mid-path (...Pipeline...); preserve only the visible portion.