Headquartered in Wilmington, United States, Clovis Oncology, Inc. belongs to the Healthcare & Pharma sector and traces its origins to 2009. Filings by its managers are published through SEC (Form 4). No insider at Clovis Oncology, Inc. has published a filing in the past twelve months. The most recent one dates from 3 November 2022.
Our records for Clovis Oncology, Inc. go back to 2017, with 14 purchases and 293 sales on the open market in total.
This summary is built from SEC (Form 4) disclosures alone and does not predict where the share price will go.
FY ended December 2021 · cache
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Clovis Oncology, Inc. was a U.S.-based biopharmaceutical company focused on oncology precision medicine and historically listed on the NASDAQ market in the United States. Founded in 2009 and long headquartered in Boulder, Colorado, the company built its business model around acquiring, developing, and commercializing anti-cancer therapies aimed at well-defined patient subgroups, often in combination with companion diagnostics. Its best-known commercial asset was Rubraca® (rucaparib), an oral PARP inhibitor used in specific oncology indications, including certain ovarian cancer settings and, at one point, metastatic castration-resistant prostate cancer. ([sec.gov](https://www.sec.gov/Archives/edgar/data/1466301/000156459016013672/clvs-10k_20151231.htm?utm_source=openai))
From an industry perspective, Clovis belonged to the specialized biotech segment, where value creation depends on clinical differentiation, regulatory execution, and the ability to serve niche oncology populations. The company’s legacy footprint extended beyond the United States, with operations and additional offices in Europe, including Cambridge in the United Kingdom and Milan, Italy. That international setup reflected its ambition to develop and commercialize oncology assets across the U.S., Europe, and other markets. Its competitive set included other PARP inhibitor developers, targeted oncology biotechs, and larger pharmaceutical groups active in precision cancer care. ([sec.gov](https://www.sec.gov/Archives/edgar/data/1466301/000156459016013672/clvs-10k_20151231.htm?utm_source=openai))
Clovis’s corporate trajectory is also defined by financial stress and restructuring. The company and certain subsidiaries filed voluntary Chapter 11 petitions in December 2022 in the U.S. Bankruptcy Court for the District of Delaware. The court later confirmed the company’s Third Amended Joint Chapter 11 Plan of Liquidation in June 2023, with an effective date of July 10, 2023. For equity investors, that is a critical point: the company’s public-market story is no longer one of normal growth execution, but of restructuring and asset disposition. ([sec.gov](https://www.sec.gov/Archives/edgar/data/1466301/000119312522303179/d386858dex991.htm?utm_source=openai))
In analytical terms, Clovis was a classic high-risk oncology biotech: concentrated product exposure, heavy clinical and regulatory dependence, and significant financing vulnerability. The most recent material developments therefore center on bankruptcy proceedings and asset sales rather than product launches or commercial acceleration. ([sec.gov](https://www.sec.gov/Archives/edgar/data/1466301/000119312523094018/d492602d8k.htm?utm_source=openai))
Headquarters: Wilmington, United States · Founded: 2009 · Wikipedia article
Source: Wikidata (CC0).
| Fiscal year end | Revenue | Net income | Diluted EPS | Filing |
|---|---|---|---|---|
| Dec 2021 | 148.8 m USD | -264.5 m USD | -2.29 USD | 10-K |
| Dec 2020 | 164.5 m USD | -369.2 m USD | -4.38 USD | 10-K |
| Dec 2019 | 143.0 m USD | -400.4 m USD | -7.43 USD | 10-K |
| Dec 2018 | 95.4 m USD | -368.0 m USD | n.d. | 10-K |
| Dec 2017 | 55.5 m USD | -346.4 m USD | n.d. | 10-K |
Amounts in USD, as filed (forms 10-K, 20-F or 40-F). Source: SEC EDGAR.