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3 stories mentioning ARVNUpdated 34d ago

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Wire

Arcus Biosciences' Casdatifan Therapy Could be Launched in 2028, Morgan Stanley Says

Arcus Biosciences (RCUS) Casdatifan therapy for renal cell carcinoma could be launched in 2028 and potentially generate $1.40 billion in unadjusted revenue by 2035, Morgan Stanley said in a Monday note.The estimates are risk-adjusted based on a 60% probability of success, the brokerage said. Arcus is set to release further data on three Casdatifan settings in October, with each setting pairing its therapy with different antibodies, according to the note.Arcus is also on track for a readout of Quemliclustat's phase 3 trial in pancreatic cancer in H1 2027 and kickstart clinical development of its early immunology portfolio, the investment firm added.Meanwhile, Morgan Stanley projected an initial launch for Arvinas' (ARVN) investigational ARV-393 therapy for non-Hodgkin lymphoma patients in 2029. The brokerage estimates unadjusted sales of $1.30 billion by 2035, risk-adjusted using a 25% probability of success.The investment firm also noted that it adjusted its model for Arvinas to account for Veppanu royalties and milestone payments, instead of end-user sales, given an exclusive license deal on the therapy. Veppanu is a newly approved therapy for breast cancer, according to the note.Morgan Stanley raised its price target on Arcus Biosciences to $23 from $22 and cut that of Arvinas to $10 from $11, both with an equal-weight rating.Price: $28.60, Change: $-0.02, Percent Change: -0.07%

$ARVN$RCUS
Wire

Wedbush Adjusts Price Target on Arvinas to $12 From $11, Maintains Neutral Rating

Arvinas (ARVN) has an average rating of overweight and mean price target of $15.08, according to analysts polled by FactSet.Price: $9.33, Change: $+1.27, Percent Change: +15.76%

$ARVN
Wire

Arvinas Reports FDA Approval of Veppanu for Advanced Breast Cancer

Arvinas (ARVN) and partner Pfizer (PFE) said Friday the US Food and Drug Administration has approved Veppanu for the treatment of adults with advanced breast cancer.The indication is for estrogen receptor-positive/human epidermal growth factor receptor 2-negative, estrogen receptor 1-mutated advanced or metastatic breast cancer, with disease progression following at least one line of endocrine therapy, they said.This is the first time the regulator has approved a PROteolysis TArgeting Chimera, a form of heterobifunctional protein degrader therapy, according to the release.Shares of Arvinas were up over 7%, and Pfizer was down about 1% in afternoon trading.Price: $10.64, Change: $+0.74, Percent Change: +7.47%

$ARVN$PFE

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