10-Q · May 7, 2026
Lantheus reported a solid Q1 2026 with revenue of $377.3 million, exceeding estimates and achieving an EPS of $1.80, reflecting a 62.3% increase in net income year-over-year. However, gross profit declined slightly,…
10-Q · Filed November 5, 2026 · Our reading of the company's report
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Lantheus reported third-quarter revenue of $389.9 million and diluted EPS of $0.33, with revenue modestly above both the prior quarter’s $388 million and the year-ago quarter’s $384 million. GAAP earnings remain…
Lantheus reported third-quarter revenue of $389.9 million and diluted EPS of $0.33, with revenue modestly above both the prior quarter’s $388 million and the year-ago quarter’s $384 million. GAAP earnings remain pressured by $31.0 million of intangible-asset impairments. The pending Curium merger, including the FTC’s October 21 Second Request and potential $228.0 million termination fee, remains the principal near-term uncertainty, while full-year 2026 guidance has been withdrawn.
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Third-quarter revenue was $389.9 million, up from $388 million in the prior quarter and $384 million in the year-ago quarter based on the provided quarterly history.
The company reported $96.3 million of equity investments in Perspective Therapeutics, Radiopharm Theranostics and Illuminated Holdings, exposing the balance sheet to equity-price volatility.
Lantheus received FDA approval for TAUKLARIFY on August 14, 2026 and CMS granted PYLARIFY TruVu TPT Status effective October 1, 2026, supporting its neurology and prostate-imaging portfolios.
The company received final FDA approval for BRAVNETSA on September 22, 2026, although launch timing remains subject to Hatch-Waxman litigation and commercial readiness.
The company retained $200.0 million of remaining authorization under its share-repurchase program through December 2027 and made no repurchases under that program during the three months ended September 30, 2026.
The FTC issued a Second Request on October 21, 2026, extending the HSR waiting period until 30 days after substantial compliance unless terminated sooner. The merger consideration includes $102.50 per share plus a CVR of up to $12.00, and the company may owe a $228.0 million termination fee in specified circumstances.
Third-quarter impairment charges totaled $31.0 million, including $21.0 million for LNTH-2620 and $10.0 million for LNTH-2515. Further clinical, regulatory or commercial setbacks could result in additional impairment charges.
PYLARIFY TruVu is expected to become commercially available beginning in the fourth quarter of 2026, but TPT Status is temporary and the company cannot assure timely technology transfer, PMF approvals or customer adoption.
The company withdrew previously issued full-year 2026 financial guidance because of the pending Curium merger; no replacement quantitative revenue or EPS guidance was provided.
Lantheus reported a solid Q1 2026 with revenue of $377.3 million, exceeding estimates and achieving an EPS of $1.80, reflecting a 62.3% increase in net income year-over-year. However, gross profit declined slightly,…
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Lantheus reported revenue of $372,764,000 for the three months ended March 31, 2025, up $2,789,000 versus $369,975,000 in Q1 2024, while diluted EPS fell to $1.02 from $1.87 a year ago. Gross margin was 63.8% and…
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