Financial Performance & Outlook - Alvotech's revised outlook for 2025 projects revenues between $600 million and $700 million, including product revenue of $340 million to $410 million and milestone revenues of $260 million to $290 million[12] - The company anticipates an adjusted EBITDA of $200 million to $280 million in 2025[12] - Alvotech expects a product margin of 38-41% and a gross margin of 65-66%[12] - Q1 2025 product revenue reached $110 million, a 784% increase compared to $12 million in Q1 2024[34] - Total revenue for Q1 2025 was $133 million, a 260% increase from $37 million in Q1 2024[34] Product Pipeline & Commercialization - Alvotech has a robust pipeline of biosimilar candidates, including AVT02 (adalimumab), AVT04 (ustekinumab), and others in various stages of development and commercialization[23] - The company expects >50% of the U S Humira® market to convert to biosimilars before the end of 2025[25] - SELARSDI® (Stelara® biosimilar) has been approved in the U S as an interchangeable biosimilar for all presentations[25] Cash Flow & Capital Structure - Alvotech had cash and cash equivalents of $39 million as of March 31, 2025, with total borrowings of $1,097 million[40] - The company anticipates being free cash flow positive in 2025 based on current operating plans[40] - As of March 31, 2025, there were 301.9 million common shares outstanding[40]

Core Viewpoint - The FDA has approved Teva Pharmaceutical Industries Ltd. and Alvotech's Selarsdi as an interchangeable biosimilar to Johnson & Johnson's Stelara, expanding treatment options for various inflammatory conditions [1][2]. Group 1: Product Approval and Details - Selarsdi is approved for multiple indications, including adult and pediatric psoriatic arthritis, plaque psoriasis, Crohn's disease, and ulcerative colitis, effective from April 30, 2025 [1]. - The approved presentations of Selarsdi include 45 mg/0.5 mL and 90 mg/mL in prefilled syringes, 45 mg/0.5 mL in vials, and 130 mg/26 mL for intravenous infusion [3]. Group 2: Strategic Partnerships and Market Position - Teva and Alvotech entered a strategic partnership in August 2020 to exclusively commercialize five biosimilar candidates, which was later extended to include additional products [4]. - Teva's recent launches of Selarsdi and another biosimilar, along with a robust pipeline, position the company for strong leadership in the biosimilars market [2]. Group 3: Financial Impact and Stock Performance - Following the news of the approval, TEVA stock increased by 2.10% to $16.53, while ALVO stock rose by 0.67% to $8.22 [5]. Group 4: Future Developments - The FDA has accepted Biologics License Applications for three additional biosimilar candidates developed by Alvotech in partnership with Teva, with goal dates for approval in Q4 2025 [6].

Financial Performance & Outlook - Total revenues reached $492 million, exceeding the latest guidance, compared to $93 million in 2023, a 427% increase[25,59] - Product revenues were $273 million, surpassing $49 million in 2023, a 462% increase[25,59] - Adjusted EBITDA was $108 million, a significant turnaround from a loss of $291 million in 2023[25,59] - The company anticipates revenues between $570 million and $670 million in 2025, with product revenue contributing $340 million to $410 million and milestone revenues between $230 million and $260 million[67] - The company projects an adjusted EBITDA between $180 million and $260 million in 2025[67] - Alvotech targets approximately $1.5 billion in revenue by 2028[70,77] - Alvotech targets an EBITDA margin of 40-45% by 2028[73,77] Commercial & R&D Updates - SIMLANDI units shipped to the US across both branded and private label channels in 2024 reached 1.3 million, with 60% of those units shipped in Q4 2024[35] - The company has biosimilar approval in 63 markets and has launched in 29 markets[37] - By the end of 2025, investments will enable a total annual capacity of 15 million finished units[42]