Arvinas announces that its second targeted protein degrader has entered the clinic: ARV-471 for the potential treatment of patients with locally advanced or metastatic ER positive / HER2 negative breast cancer.

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30 Mar 2021 1 dose escalation data on protein degrader ARV-471 for breast cancer the stock could trade up meaningfully as ARV-471will be positioned 

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Arv 471

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Jul 1, 2020 product candidates, ARV-110 and ARV-471, and the timing of clinical trials and data from those trials for our product candidates, and our 

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Arv 471

Karl Arv. Arb. Hornsg.

Arv 471

Part A: Assessment of anti-tumor activity of ARV-471, 28 Days. 471. Preskriptionsfristen för rätt till återvinning av arvsskatt räknas från den dag då den för högt beräknade skattskyldigheten slutligen fastställdes. Utlänning äger i Finland samma rätt till arv som finsk medborgare.
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About Arvinas ARV-471, an estrogen receptor (ER) alpha PROTAC, is a hetero-bifunctional molecule that facilitates the interactions between estrogen receptor alpha and an intracellular E3 ligase complex, leading to the ubiquitylation and subsequent degradation of estrogen receptors via the proteasome. ARV-471 robustly degrades ER in ER-positive breast cancer cell ARV-471 is a clinical stage, oral PROTAC ® degrader that targets the estrogen receptor (ER), a highly validated driver of breast cancer. More information is available here. ARV-766 is an oral PROTAC ® protein degrader that targets the androgen receptor (AR) and has a different profile than ARV-110. Both ARV-471 and ARV-110 have been well tolerated, neither has reached a maximum tolerated dose, and the Phase 1 dose escalation trials for both programs continue.

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2020-05-13 · Combination therapy of ARV-471 with a CDK4/6 inhibitor showed more pronounced antitumor activity. Moreover, in PDX models of hormone-independent breast cancer with ERα mutations, treatment with ARV-471 in a dose of 10 mg/kg completely inhibited tumor growth accompanied with significantly reduced mutant ER levels.

ARV-766 is an oral PROTAC ® protein degrader that targets the androgen receptor (AR) and has a different profile than ARV-110.