Insmed [INSM]
Spot $103.16 (2026-07-29). No position verdict is issued — the memo scores criteria; the book decides. What follows is the construction that would apply, and the vehicle argument.
Equity is the default and needs no argument. A LEAP was nevertheless tested against the standard — measured IV minus trailing 252-day realised vol — and fails:
| Trailing 252-day realised volatility | 54.1% |
| Measured IV, INSM 2027-08-20 $105 call | 62.7% |
| Measured IV, INSM 2027-11-19 $105 call | 61.7% |
| IV − realised | +8.6pp — options are expensive |
Constructability also fails at the strike. The 2027-08-20 $105 call quotes $25.33 bid / $28.65 ask, a 12.3% of mid spread, with quoted size 5 x 7 contracts. Open interest across the entire $95–$115 strike range for both 2027 expiries is 5 contracts on one line and reported as null on the other eleven. There is no size available at any reasonable price. Multi-leg is therefore also inadmissible: the requirement is constructability at the strike, with quoted size, and it does not exist.
Vehicle: common stock. No options.
Position size is constrained by the cash-runway and refinancing clock, not by liquidity. Average daily volume on the last two sessions was 126,627 and 140,685 shares, roughly $13–15m/day at $103 — thin for a $22.4bn market cap, which means an exit takes days, not hours. Size to what can be exited inside the two-day window around a Q2 print.
| Level | Basis | |
|---|---|---|
| Spot | $103.16 | Alpaca close 2026-07-29 |
| Post-approval price range | $91.88 – $211.41 | Daily closes since 2025-08-12, 242 sessions |
| Post-approval median | $146.25 | same |
| Drawdown from post-approval high | −51.2% | $211.41 → $103.12 |
| 12-month target | $122.61, +18.9% | Constant 9.40x EV/NTM sales, revenue window rolled to FY2027 consensus. See INSM_Valuation.md §5 |
The stock is 51.2% off its post-approval high and within 12.3% of its post-approval low. That is the setup: the market has already taken out the launch-euphoria premium. The implied-path test says it has not taken out enough.
That the reimbursable bronchiectasis population is closer to the FDA's 500,000 than to the EC's and MHRA's frequent-exacerbator restriction. Everything else — the ARIKAYCE label expansion, TPIP's four Phase 3 programmes, the gene therapies — is second-order against that single question, and the valuation section shows the price already requires the optimistic answer plus a 78.3% terminal operating margin.