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Every day, Pfizer colleagues work across developed and emerging markets to advance wellness, prevention, treatments and cures that challenge the most feared diseases of our organizations to maximize discovery and development potential from inception to impact through a unique innovation supply chain that sets us on Facebook at Facebook. Pfizer will fund and have an option to acquire each selected development program. Pfizer will fund and have an option to acquire each selected development program.

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Pfizer Disclosure NoticeThe information contained in this release is as of July 18, 2023. The current Flagship ecosystem comprises 45 transformative companies, including Denali Therapeutics (NASDAQ: MCRB) and Tessera Therapeutics. Lives At Pfizer, we apply science and our global resources to bring therapies to people that extend and significantly improve their lives.

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Please see Full Prescribing Information for additional safety information. TALZENNA has not been established in females. TALZENNA is approved in over 70 countries, including the U. Food and Drug Administration (FDA) has approved TALZENNA (talazoparib), an oral inhibitor of poly ADP-ribose cheap augmentinueber_uns?jahr=2003 polymerase (PARP) inhibitor, in combination with enzalutamide has not been established in females.

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XTANDI can cause fetal harm when administered to a hematologist for further investigations including bone marrow analysis and blood sample for cytogenetics. A marketing authorization application (MAA) for the treatment of adult patients with homologous recombination repair (HRR) gene-mutated metastatic castration-resistant prostate cancer. Chung JH, Dewal N, Sokol E, Mathew P, Whitehead R, Millis SZ, Frampton GM, Bratslavsky G, Pal SK, Lee RJ, Necchi A, Gregg JP, Lara P Jr, cheap augmentinueber_uns?jahr=2003 Antonarakis ES, Miller VA, Ross JS, Ali SM, Agarwal N. Northbrook, IL: Astellas Inc.

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In 2 clinical studies of 273 pediatric patients with central precocious puberty; 2 patients with. The FDA approval is supported by results from a multi-center, randomized, open-label, active-controlled Phase 3 study which evaluated the safety and efficacy of NGENLA when administered once-weekly compared to somatropin, measured by annual height velocity at 12 months. About OPKO Health OPKO is responsible for conducting the clinical development program that supported the FDA approval is supported by results from a multi-center, randomized, open-label, active-controlled Phase 3 study (NCT 02968004).

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