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Rhythm Pharmaceuticals, Inc.
NASDAQ: RYTM Healthcare Pharma 🔎 Screen
🏹 Trader: 🎯 Near 52W High | BRS 71 Forming View all →
$7.2B
Market Cap
P/E
PEG
-481.1%
ROCE
-90.5%
ROE
0.01
D/E
-101.2%
OPM
-5.3%
% from 52W High
70
α RS
🔍 RYTM is showing a near-52W-high setup because it's within 5.3% of its 52-week high, RS Rating is 70, and an ECS of 66.6 last quarter. Net: Broad signal stack, not a recommendation. ? 52W High RS Rating ECS
Sources
5.3% from 52W high · RS Rating 70 · ECS 66.6
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🌏 Global Investor Returns
Currency-adjusted total returns for RYTM including FX impact
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📈 Price History
Ratio Health
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About

Rhythm Pharmaceuticals, Inc., a commercial-stage biopharmaceutical company, focuses on the rare neuroendocrine diseases in the United States and internationally.

Key Ratios Snapshot
📈 Growth Pattern
📊 Quick Scorecard
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⭐ Superinvestors Holding RYTM
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Manager Shares Value % of Fund Period
Steve Cohen Point72 Asset Management 846.8K $73.6M 0.09% Mar 2026
Jim Simons Renaissance Technologies LLC 258.0K $22.4M 0.04% Mar 2026

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

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📊 MIXED Rhythm Pharmaceuticals Q1 2026 revenue $60M, 150+ start forms for acquired HO launch
Revenue & Profitability
Global net revenues were $60.1 million in Q1 2026, representing 5% sequential growth over Q4 2025. GAAP net loss per basic and diluted share was $0.83, including $0.02 per share from accrued dividends. Non-GAAP operating expenses for Q1 were $82.2 million. The company ended the quarter with approximately $341 million in cash and equivalents.
Outlook
Management expressed confidence in the growing demand for IMCIVREE in HO, citing high unmet need and positive early payer receptivity. They noted that disease awareness continues to improve, leading to more diagnosed patients. For Japan, the PMDA has accepted the filing and approval is anticipated by year-end 2026. No macro headwinds were discussed.
Growth Drivers
The primary growth driver is the U.S. launch of IMCIVREE for acquired HO, with more than 150 patient start forms in the first six weeks and approximately 110 unique prescribers. International expansion, particularly in Japan (5,000-8,000 patient opportunity) and Europe (10,000 patients), provides additional growth. BBS revenues continue to show steady growth. Pipeline programs (RM-718, bivamelagon) represent future potential.
Balance Sheet & CapEx
Not discussed in this earnings call.
Margins
Gross-to-net for U.S. sales was 84% in Q1, consistent with recent quarters. Cost of goods sold was 11.9% of product revenue. Non-GAAP operating expense guidance for fiscal 2026 remains $385-$415 million, with quarterly spending expected to increase due to investments in CMC, clinical trials, and the Japanese team build-out.
Key Risks
Key risks include payer reimbursement timelines for HO (expected three to nine months for policy establishment), variability in patient transitions off the bridge program, and the uncertainty of early launch trajectory. Clinical trial data for pipeline candidates (RM-718, bivamelagon) remain unproven in later-stage studies. The company noted that some patients on the bridge program during Q1 2026 have since returned to reimbursed therapy.
Generated by AI · Q1 2026 results · Not investment advice
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✓ 📞 Earnings Call Transcripts (5 quarters) submit a missing quarter
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📞 Earnings Call Transcripts (5)
Q2 2026 Q2 2026 2026-08-04
IMCIVREE's U.S. launch for acquired hypothalamic obesity drove strong Q2 sales growth, with robust early demand, broad prescriber engagement, and positive payer response. International expansion and next-generation MC4R agonist development are progressing, supporting long-term growth.
Q1 2026 Q1 2026 2026-05-05
Q1 2026 saw $60.1M in revenue, driven by BBS and a strong U.S. launch of IMCIVREE for acquired HO, with over 150 start forms and positive payer response. International expansion advanced with EU approval and Japan NDA filing, supporting a robust outlook for 2026.
Q4 2025 Q4 2025 2026-02-26
IMCIVREE revenues grew 50% year-over-year to $194.8M in 2025, driven by U.S. and international expansion. Regulatory milestones for HO and new geographies are on track for 2026, with increased investment in R&D and commercial operations.
Q3 2025 Q3 2025 2025-11-04
Q3 revenue grew 54% year-over-year to $51.3M, driven by Imcivree and patient growth. Cash reserves of $416M provide 24 months of runway as the company prepares for the HO launch, with FDA approval expected by December and international expansion underway.
Q2 2025 Q2 2025 2025-08-05
Q2 2025 saw strong revenue growth, positive clinical milestones, and a strengthened balance sheet with a $189M equity raise. IMCIVREE sales expanded in both U.S. and international markets, and regulatory filings for setmelanotide in HO remain on track.
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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:
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No Investment Recommendation:
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Information Sources:
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