Daily Newsletter

14 November 2023

Daily Newsletter

14 November 2023

FDA approves Takeda’s targeted therapy for advanced colon cancer

GlobalData analysts predict sales of Takeda's Fruzaqla to reach $340m by 2028.

GlobalData Healthcare November 13 2023

On 8 November, Takeda announced it had received US Food and Drug Administration (FDA) approval for its oral Fruzaqla (fruquintinib) as a third-line treatment for adults with metastatic colorectal cancer (mCRC).

Fruzaqla is an inhibitor of all three VEGF receptor kinases and is indicated for patients already treated with fluoropyrimidine, oxaliplatin, and irinotecan chemotherapy, an anti-VEGF therapy and if medically appropriate, an anti-EGFR therapy.

Fruquintinib was developed and marketed in China by Hong Kong-based Hutchmed in 2018. Takeda acquired its ex-China rights in January of this year for an upfront payment of $400m.

The approval of Fruzaqla is based on data from Phase III trials FRESCO-2 and FRESCO, the latter conducted in China alone.

In FRESCO-2, patients with refractory mCRC who received Fruzaqla showed a median overall survival (OS) rate of 7.4 months versus 4.8 months in the placebo group (hazard ratio/HR: .66).

Grade three or higher adverse events occurred in 63% of patients in the treatment group versus 50% in the placebo.

The results were consistent with the FRESCO trial where patients were treated with Fruzaqla after two prior lines of chemotherapy.

The median OS there was 9.3 months versus 6.6 months for placebo (HR: .65). The median progression-free survival also significantly increased at 3.7 months versus 1.8 months.

In the US, GlobalData epidemiologists estimate 143,000 people will be diagnosed with mCRC in 2023 at a 1.4% annual growth rate until 2031.

The chemotherapy-free Fruzaqla, marketed as Elunate in China by Eli Lilly, will compete with Taiho and Servier’s chemotherapy Lonsurf in combination with the targeted therapy bevacizumab.

GlobalData analysts forecast sales for Lonsurf to reach $633m by 2028.

Additional competition will come from Bayer’s kinase inhibitor Stivarga (regorafenib), which registered $645m in sales last year.

Takeda has applications in place for Fruzaqla’s approval in Europe and Japan and is investigating the drug in Phase II trials for endometrial and triple-negative breast cancer.

GlobalData analysts anticipate sales for Takeda’s Fruzaqla to reach $340m by 2028.

Disease-modifying therapies (DMTs) entering the PD market pose significant opportunities and risks

As PD therapy currently centers on symptomatic treatment, the need for DMTs is one of the greatest unmet needs. Several companies within the late-stage PD pipeline are developing drugs that target PD via novel MOAs. Targeting α-synuclein and other neurotoxic proteins is a key strategy in the late-stage pipeline for DMTs. However, the lack of validated predictive biomarkers of PD progression have made the development of DMTs and neuroprotective agents challenging.

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