RE: Another cancer treatment reported2 Jun 2026 09:28
Thank you guys. Ai makes it sound like 6000 isn’t as good.
Emi-Le (Servier – ACC)
* ORR: 35.6% overall (46.9% in higher-risk ACC subgroup)
* Median PFS: 7.8 months (mature Phase 1 readout)
* Well-defined ACC population
* Endpoints are fully calculable and stable
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AVA6000 (Avacta – salivary gland cancers)
Phase 1a (~11 patients)
* ORR: very limited numbers (small cohort; early responses only)
* Median PFS: ~9 months (very small n, early signal only)
Phase 1b (expansion cohort – ongoing)
* ORR: ~10% overall response rate reported so far
* Disease control: ~90–92%
* Median PFS: not yet mature / not formally established
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Direct comparison
ORR
* Emi-Le: ~36–47% (strong, consistent response rate in ACC)
* AVA6000: ~10% (early expansion signal, broader population)
👉 Clear advantage:
Emi-Le (significantly higher response rate and more defined dataset)
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PFS
* Emi-Le: 7.8 months (confirmed median)
* AVA6000: ~5–9 month early range, not a final median
👉 Clear advantage:
Emi-Le (because it has a mature, reportable median PFS)
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Overall interpretation (biased toward Emi-Le)
Even allowing for early-stage uncertainty:
Emi-Le is stronger because:
* Higher ORR (~36–47% vs ~10%)
* Mature, reportable PFS (7.8 months)
* Clean ACC-specific dataset
* More statistically reliable Phase 1 readout
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AVA6000 profile right now:
* Lower early ORR (~10%)
* PFS still evolving (no confirmed median in full dataset)
* Data still split across Phase 1a + ongoing Phase 1b expansion
* Potential signal exists, but not yet mature or competitive on headline efficacy metrics
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Bottom line
Based on current available data, Emi-Le shows a stronger and more mature efficacy profile than AVA6000, particularly on ORR and PFS consistency, while AVA6000 remains earlier-stage with a modest (~10%) emerging response rate and immature survival data