Phase 3AGIONCT07174336

A Study of Tersolisib (LY4064809/STX-478) With Other Anti-Cancer Treatments in Participants With Advanced Breast Cancer FDA Decision: Agios Pharmaceuticals (AGIO)

Decision Date
May 1, 2029

Drug Overview

Drug / TherapyA Study of Tersolisib (LY4064809/STX-478) With Other Anti-Cancer Treatments in Participants With Advanced Breast Cancer
Indication
Decision TypePhase 3
Trial PhasePhase 3
ClinicalTrials.govNCT07174336

Company Overview

Agios Pharmaceuticals (AGIO) operates in the Rare Disease sector. The current BTS Score is 86 (Grade: A).

Dilution Risk Assessment

Biotech companies frequently raise capital through secondary offerings, ATM programs, and convertible notes. Before or after major FDA decisions, dilution events are common. Understanding a company's dilution history is critical for managing risk around catalyst dates.

Frequently Asked Questions

Q:When is the Phase 3 date for A Study of Tersolisib (LY4064809/STX-478) With Other Anti-Cancer Treatments in Participants With Advanced Breast Cancer ?

The Phase 3 date for A Study of Tersolisib (LY4064809/STX-478) With Other Anti-Cancer Treatments in Participants With Advanced Breast Cancer by Agios Pharmaceuticals (AGIO) is scheduled for May 1, 2029. This is the target date for the FDA to make a decision on this application.

Q:What is A Study of Tersolisib (LY4064809/STX-478) With Other Anti-Cancer Treatments in Participants With Advanced Breast Cancer used for?

A Study of Tersolisib (LY4064809/STX-478) With Other Anti-Cancer Treatments in Participants With Advanced Breast Cancer is being developed by Agios Pharmaceuticals for the treatment of its target indication. It is currently in Phase 3 clinical trials.

Q:What happens if A Study of Tersolisib (LY4064809/STX-478) With Other Anti-Cancer Treatments in Participants With Advanced Breast Cancer gets FDA approval?

If A Study of Tersolisib (LY4064809/STX-478) With Other Anti-Cancer Treatments in Participants With Advanced Breast Cancer receives FDA approval, Agios Pharmaceuticals (AGIO) would be able to market the drug in the United States for its target indication. This typically leads to significant stock price movement for biotech companies. Investors should monitor the Phase 3 date closely.

Q:What is the dilution risk for AGIO?

Biotech companies often raise capital through share offerings, which can dilute existing shareholders. You can check the current dilution risk for AGIO on DilutionWatch at dilutionwatch.com/stock/AGIO.html.

Q:Where can I find more information about Agios Pharmaceuticals?

You can view the full BiotechSigns company profile for Agios Pharmaceuticals (AGIO) at biotechsign.com/app/company/AGIO, which includes the BTS Score, signal history, clinical trial data, and insider trading activity.

Disclaimer

This page is for informational purposes only and does not constitute investment advice. FDA decision dates are subject to change. Clinical trial outcomes are inherently uncertain. Biotech stocks are highly volatile — past performance does not guarantee future results. Always consult a qualified financial advisor before making investment decisions. BiotechSigns is not a registered investment advisor.