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KalVista Pharmaceuticals, Inc.
NASDAQ: KALV Healthcare Pharma 🔎 Screen
🏹 Trader: 🎯 Near 52W High View all →
$1.4B
Market Cap
P/E
PEG
-1,158.3%
ROCE
N/M
ROE
0.05
D/E
OPM
0.0%
% from 52W High
90
α RS
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🌏 Global Investor Returns
Currency-adjusted total returns for KALV including FX impact
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📈 Price History
Ratio Health
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About

KalVista Pharmaceuticals, Inc., a biopharmaceutical company, develops oral therapies for individuals for rare diseases with unmet needs.

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Manager Shares Value % of Fund Period
Steve Cohen Point72 Asset Management 2.14M $43.0M 0.06% Mar 2026

SEC Form 13F data. 45-day lag from quarter end.

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📊 MIXED KalVista's EKTERLY achieves $13.7M in first three months, 937 start forms in U.S.
Revenue & Profitability
For the three months ended September 30, 2025, KalVista reported EKTERLY sales of $13.7 million. Total operating expenses were $59.7 million, consisting of approximately $12 million in R&D and $46.5 million in SG&A. Gross-to-net was toward the low end of the expected range (upper teens low 20s) due to lower copay utilization. Net income or operating income was not disclosed; the company stated its cash position is sufficient to fund operations through profitability.
Outlook
Management expressed strong confidence in the long-term adoption of oral on-demand therapies to displace injectables. They noted that the early launch data validates the existence of a high-burden patient population that was previously underserved. The company sees growing prescriber confidence and expects formal payer coverage to solidify by early 2026, with policies largely favorable (PA to label).
Growth Drivers
Key growth drivers include the continued U.S. launch, expanding beyond high-burden patients to the broader HAE population, and global expansion. Germany launched in October 2025 with first-day commercial sales. The U.K. launch is expected in H1 2026 after NICE discussions. Japan launch is anticipated in Q1 2026 via partner Kaken Pharmaceutical. A pediatric NDA submission is planned for Q3 2026.
Balance Sheet & CapEx
Not discussed in this earnings call.
Margins
Gross-to-net was toward the low end of the expected range (upper teens low 20s) this quarter, driven by lower copay utilization typical for the period. Management expects SG&A expenses to remain relatively consistent as they invest in the global launch. No specific margin guidance was provided, but the company stated it is fully financed through profitability.
Key Risks
Risks highlighted include potential seasonal slowdown in demand during the holiday period (November/December) due to physician and patient time constraints. Payer access dynamics, such as quantity limits and step-through requirements, are being managed but remain a factor. The company also noted that as adoption expands beyond high-burden patients, refill rates and volumes may normalize to lower levels.
Generated by AI · Q3 2026 results · Not investment advice
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✓ 📞 Earnings Call Transcripts (2 quarters) submit a missing quarter
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📞 Earnings Call Transcripts (2)
Q3 2026 Q3 2026 2025-11-11
EKTERLY's launch drove $13.7M in sales with rapid adoption among high-burden HAE patients and strong refill rates. International expansion is progressing, and payer access is broadening, supporting expectations for EKTERLY to become the foundational HAE therapy.
Q1 2026 Q1 2026 2025-09-11
EKTERLY's U.S. launch saw rapid adoption, with nearly 5% of the HAE population submitting prescriptions and $1.4M in net revenue. International regulatory progress is strong, and cash reserves are expected to fund operations into 2027. Early safety and access signals remain positive.
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📊 Analysis Methodology

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Financial Model
Projections are built from each company's audited annual financials (Income Statement, Balance Sheet, Cash Flow) over the last 5 fiscal years. Forward assumptions — revenue growth %, EBITDA margin, D&A (USD millions), interest expense, tax rate, and capex — are AI-generated using historical context and refreshed twice a year: after the December results season and after the September/Q4 results season.

DCF Valuation
Fair Value = Σ(FCFt / (1+WACC)t) + Terminal Value. Terminal Value uses the Gordon Growth Model: FCF5 × (1+g) / (WACC−g). Default WACC: 10% (US risk-free ~4.5%, equity risk premium ~5.5%). Default terminal growth: 3% (long-run US nominal GDP proxy).

CAGR Tracker
Expected 5-year CAGR = (DCF Fair Value / Current Price)1/5 − 1. Assumes fair value is reached in exactly 5 years — a mechanical estimate only.

Data Sources & Limitations
Financial statements sourced from public filings. Prices updated daily. Forward assumptions are AI-generated. All monetary values in USD millions. Non-US ADR companies may have currency conversion inaccuracies. Models are point-in-time and do not update intra-quarter or account for M&A, macro shocks, or extraordinary items.

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Investment Risk:
Investing in securities, including US equities and ETFs, involves inherent risks including the potential loss of principal. All investments are subject to market fluctuations, economic conditions, regulatory changes, and other factors that may affect their value. Past performance is not indicative of future results. This analysis is provided for informational and educational purposes only and should not be construed as investment advice under any circumstances.

No Investment Recommendation:
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Information Sources:
The analysis is based on publicly available information including SEC filings (10-K, 10-Q), annual reports, management commentary, and publicly available financial data. Information is believed to be accurate as of the date of publication but may be subject to change without notice. Readers are encouraged to independently verify all information before acting upon it.

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