CTI BioPharma Corp. was a biopharmaceutical company dedicated to the acquisition, development, and commercialization of novel targeted therapies for blood-related cancers and other rare diseases. Its primary product, VONJO® (pacritinib), received FDA approval for treating adult patients with intermediate or high-risk primary or secondary (post-polycythemia vera or post-essential thrombocythemia) myelofibrosis with a platelet count below 50 × 10⁹/L. In June 2023, CTI BioPharma was acquired by Swedish Orphan Biovitrum AB (Sobi) for $1.7 billion and now operates as a key part of Sobi's portfolio in rare disease and specialty care, particularly strengthening its hematology franchise.
Historically, the Seattle headquarters served as the nerve center for CTI BioPharma's corporate strategy, research and development oversight, clinical trial management, and commercial preparation.
The headquarters was situated in a modern office building in a key business district, offering advanced facilities conducive to a biotech firm. Specific unique architectural highlights were not a primary public feature.
The work culture at CTI BioPharma, typical for a dynamic biopharmaceutical company, likely emphasized scientific innovation, patient focus, collaboration among multidisciplinary teams, and a results-oriented approach to drug development.
This headquarters was central to the successful development, FDA approval, and initial commercialization of VONJO®, representing a major milestone for the company and a new therapeutic option for myelofibrosis patients.
Prior to its acquisition by Sobi, CTI BioPharma maintained a strategic global presence focused on North America and Europe. Its activities encompassed multinational clinical trials, engagement with global regulatory authorities like the FDA and EMA, and building the groundwork for international commercial operations for its therapies, primarily VONJO®.
3101 Western Avenue, Suite 800
Seattle
WA
USA
Address: Via Mike Bongiorno 13, 20124 Milan, Italy
To support CTI BioPharma's strategic objectives in Europe, including engagement with the European Medicines Agency (EMA) and establishing a presence in key European markets for its therapeutic candidates.
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As of April 2025, CTI BioPharma' leadership includes:
CTI BioPharma has been backed by several prominent investors over the years, including:
The most significant event impacting CTI BioPharma's executive team in the last 12 months was its acquisition by Sobi, completed in June 2023. This led to the transition of CTI BioPharma's leadership as the company and its operations were integrated into Sobi's global structure. Consequently, the former CTI executive team largely departed from their roles within the independent CTI entity.
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Prior to its acquisition by Sobi in June 2023, CTI BioPharma likely used standard corporate email formats such as [first_initial][last]@ctibiopharma.com. Following the acquisition, emails to the `ctibiopharma.com` domain may be inactive or redirected. For current business communications related to former CTI BioPharma assets, refer to Sobi's official contact channels.
[first_initial][last]@ctibiopharma.com
Format
jdoe@ctibiopharma.com
Example
10%
Success rate
Sobi • June 3, 2024
Sobi announced updated results from an indirect comparison of overall survival (OS) in patients with cytopenic myelofibrosis treated with pacritinib (VONJO) versus real-world data (RWD) on best available therapy (BAT). The findings were presented at the 2024 American Society of Clinical Oncology (ASCO) Annual Meeting....more
Sobi • June 26, 2023
Sobi (Swedish Orphan Biovitrum AB) announced the successful completion of its recommended cash offer to acquire CTI BioPharma Corp. for $9.10 per share, representing an equity value of approximately $1.7 billion. This acquisition strengthens Sobi's position in rare hematology....more
CTI BioPharma (via PR Newswire) • February 28, 2022
CTI BioPharma Corp. announced that the U.S. Food and Drug Administration (FDA) granted accelerated approval to VONJO (pacritinib) for the treatment of adult patients with intermediate or high-risk primary or secondary myelofibrosis with a platelet count below 50 × 10⁹/L....more
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