Investor Presentation January 2026 © 2026 EyePoint. All Rights Reserved. Legal Disclaimers Various statements made in this presentation are forward-looking, within the meaning of the U.S. Private Securities Litigation Reform Act of 1995, and are inherently subject to risks, uncertainties and potentially inaccurate assumptions. All statements that address activities, events or developments that we intend, expect, plan or believe may occur in the future, are forward-looking statements, including but not limit ...

Corporate Presentation January 2026 © 2026 ANI Pharmaceuticals, Inc. 1 Disclaimers Forward-Looking Statements This presentation contains forward-looking statements within the meaning of Section 27A of the Act, and Section 21E of the Securities Exchange Act of 1934, as amended. The guidance included herein is from or supplemental to the Company's press release on January 12, 2026. The Company is neither reconfirming this guidance as of the date of this investor presentation nor assuming any obligation to upd ...

Corporate Presentation for JPM January 2026 Forward-Looking Statements This presentation contains "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995, as amended (the "Act"). Forward-looking statements are statements that are not of historical fact and include, without limitation, statements regarding future events, our future financial condition, results of operations, business strategy and plans, prospective products (as well as their potential to achiev ...

IBTROZI (Taletrectinib) - IBTROZI is a next-generation ROS1 inhibitor approved for advanced ROS1+ NSCLC in the U S, Japan, and China[3] - The U S FDA approved IBTROZI on June 11, 2025[117, 120] - Since its U S launch, IBTROZI has achieved 432 new patient starts[16, 20, 120] - IBTROZI has a theoretical maximum gross market opportunity of approximately $4 billion[16] - Median Duration of Response (DOR) in TKI-naïve patients reached 50 months[24, 25] - Nuvation Bio entered an exclusive licensing agreement with Eisai for IBTROZI in Europe and additional countries, receiving up to ~$230 million in cash consideration[6] Safusidenib - Safusidenib is a potentially best-in-class mIDH1 inhibitor being evaluated in a pivotal study for high-grade and high-risk IDH1-mutant glioma[3, 4, 118, 120] - A Phase 1 study of Safusidenib in high-grade IDH1-mutant glioma showed a 17% confirmed objective response rate (cORR), including 2 complete responses (CRs)[83, 84] - A Phase 2 study of Safusidenib in low-grade IDH1-mutant glioma showed a 24-month progression-free survival (PFS) rate of 88%[71, 83, 84] Financial Status - Nuvation Bio has a robust pro forma cash balance of approximately $589 million, expected to provide a path to profitability without needing additional funding[3, 119]

NASDAQ: CPRX January 2026 Improving the Lives of Patients Living with Rare Diseases Safe Harbor This presentation contains forward-looking statements that are subject to a number of risks and uncertainties, many of which are outside our control. All statements regarding our strategy, future operations, financial position, estimated revenues or losses, projected costs, prospects, plans, and objectives, other than statements of historical fact included in our filings with the U.S. Securities and Exchange Comm ...

ARCALYST Performance and Market - ARCALYST has achieved approximately $1.5 billion in net revenue since its launch and is on track to become a blockbuster[7] - ARCALYST has only about 18% penetration into the multiple recurrence population, indicating continued growth potential[7] - The company anticipates ARCALYST revenue between $900 million and $920 million in 2026[7] - Approximately 80% of patients on ARCALYST were prescribed the drug when they had 2 or more recurrences, while about 20% were prescribed on their 1st recurrence[27] - In Q4 2025, ARCALYST net revenue reached $202.1 million, representing approximately 65% year-over-year growth[32] Financial Position and Pipeline - The company reported approximately $414 million in cash reserves at the end of 2025[8] - KPL-387, is currently in a Phase 2/3 trial, with Phase 2 data expected in the second half of 2026[7] - KPL-1161 Phase 1 first-in-human trial is expected to initiate by the end of 2026[7] KPL-387 Development - Approximately 75% of recurrent pericarditis patients prefer the KPL-387 target profile over available commercial and investigational therapies[58] - Approximately 75% of ARCALYST-naïve patients would be more willing to take an injectable therapy if presented in an autoinjector[59] - Approximately 70% of healthcare providers report a high likelihood of prescribing KPL-387 for new patients[60]

EVERY BREAKTHROUGH BEGINS WITH BELIEF January 2026 Corporate Presentation Disclaimer Forward Looking Statements This communication contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. These statements may discuss goals, intentions and expectations as to future plans, trends, events, results of operations or financial condition, or otherwise, based on current expectations and beliefs of the management of Neurogene, as well as assumptions made by, and ...

© 2 0 2 6 O R U K A T H E R A P E U T I C S Disclaimers The information contained in this presentation has been prepared by Oruka Therapeutics, Inc. (the "Company") and contains information pertaining to the business and operations of the Company. The information contained in this presentation: (a) is provided as at the date hereof, is subject to change without notice, and is based on publicly available information, internally developed data as well as third party information from other sources; (b) does no ...

Corporate Presentation Financial Discipline and Opportunistic Innovation * RYTELO® (imetelstat) is approved in the U.S. and the EU for the treatment of certain adult patients with lower-risk myelodysplastic syndromes (LR-MDS) with transfusion-dependent anemia. See U.S. Prescribing Information and Medication Guide: https://pi.geron.com/products/US/pi/rytelo_pi.pdf; see Summary of Product Characteristics for RYTELO in the EU: https://pi.geron.com/products/rytelo/eu/rytelo_smpc_eu.pdf o $220M-$240M in expected ...

Bicycle Therapeutics Investor Presentation • January 2026 Forward-looking statements This presentation may contain forward-looking statements made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. These statements may be identified by words such as "aims," "anticipates," "believes," "could," "estimates," "expects," "forecasts", "goal," "intends," "may," "plans," "possible," "potential," "seeks," "will," and variations of these words or similar expressions that a ...