| Valuation method | Value, € | Upside, % |
|---|---|---|
| Artificial intelligence (AI) | n/a | n/a |
| Intrinsic value (DCF) | n/a | |
| Graham-Dodd Method | n/a | |
| Graham Formula | 2.10 | 2208 |
Clovis Oncology, Inc. (C6O.DE) is a biopharmaceutical company specializing in the acquisition, development, and commercialization of innovative anti-cancer therapies. Headquartered in Boulder, Colorado, the company focuses on precision medicine, primarily targeting recurrent epithelial ovarian, fallopian tube, and primary peritoneal cancers, as well as metastatic castration-resistant prostate cancer. Its flagship product, Rubraca (rucaparib), is a PARP inhibitor approved in the U.S. and Europe. Additionally, Clovis is advancing lucitanib, an angiogenesis inhibitor, and FAP-2286, a peptide-targeted radionuclide therapy, through its pipeline. The company collaborates with industry leaders like Pfizer, AstraZeneca, and Bristol Myers Squibb to enhance its research and commercialization efforts. Operating in the high-growth biotechnology sector, Clovis Oncology aims to address unmet medical needs in oncology through targeted therapies. Despite financial challenges, its focus on niche cancer treatments positions it as a potential player in the evolving precision medicine landscape.
Clovis Oncology presents a high-risk, high-reward investment opportunity in the oncology-focused biotech sector. The company's revenue of €148.8 million in FY 2021 is overshadowed by a net loss of €264.5 million, reflecting the capital-intensive nature of drug development. While Rubraca provides a revenue stream, its market penetration faces stiff competition from established PARP inhibitors. The company's pipeline, including lucitanib and FAP-2286, offers long-term potential but requires significant R&D investment. With €143.4 million in cash and €638.4 million in total debt, liquidity concerns persist. The stock's low beta (0.66) suggests relative stability, but the lack of profitability and heavy reliance on Rubraca's success make this a speculative play. Investors should weigh the potential of its clinical programs against financial sustainability risks.
Clovis Oncology operates in the highly competitive PARP inhibitor market, where it faces entrenched competitors like AstraZeneca's Lynparza and GSK's Zejula. Rubraca's differentiation lies in its specific indications, but its market share is limited compared to broader-label competitors. The company's focus on targeted therapies provides a niche advantage, but its smaller scale and financial constraints hinder aggressive commercialization. Clovis's partnerships with Pfizer and AstraZeneca bolster its R&D capabilities, yet its reliance on external collaborations exposes it to dependency risks. The development of FAP-2286 positions Clovis in the emerging radionuclide therapy space, a less saturated but unproven market. Financially, the company's significant losses and debt burden weaken its competitive standing against larger, diversified oncology players. Its survival hinges on successful pipeline progression and strategic partnerships to offset commercialization challenges.