Platform|API|Archive|Contact
Humanexa SignalsPharmaceutical Intelligence
Subscribe
Signals
Regulatory
  • FDA
  • EMA
  • MHRA
  • PMDA
  • Health Canada
Clinical
  • Phase I
  • Phase II
  • Phase III
  • Readouts
  • Enrollment Signals
Competitive
  • Pipeline Tracking
  • Company Moves
  • Asset Intelligence
  • Landscape Reports
Markets
  • Pricing
  • Access
  • Commercial
  • Launch Tracking
M&A Watch
  • Licensing
  • Acquisitions
  • Partnerships
  • Capital Raises
StrategyCatalystsPricing
Humanexa Signals

Data-driven pharmaceutical intelligence for biotech investors, pharma operators, consultants, and intelligence teams.

Powered by Humanexa

Categories

  • Regulatory
  • Clinical
  • Competitive
  • Markets
  • M&A Watch
  • Strategy
  • Catalyst Tracker

Company

  • Pricing
  • Partner with us
  • Subscribe
  • Contact
  • Privacy

Subscribe to Humanexa Signals

Weekly intelligence for pharma decision-makers.

No paywall. No spam. Unsubscribe anytime.

© 2026 Humanexa Signals. All rights reserved.

Intelligence powered by the Humanexa engine.

Asset / Drug

Astellas

Drug and asset intelligence for Astellas with 5 indexed intelligence signals across regulatory, clinical, competitive, and market developments.

Signals
5
Catalysts
0
Stage
Development stage unavailable

Sponsor company

Pfizer →

Mechanism of action

Androgen Receptor Inhibitor

Recent signals(5)

RegulatoryJuly 30, 2026

FDA Accepts Supplemental Application for XTANDI (Enzalutamide)

The FDA has accepted a supplemental application for XTANDI (enzalutamide) from Astellas.

RegulatoryJuly 29, 2026

FDA Accepts Supplemental Application for XTANDI (Enzalutamide)

The FDA has accepted a supplemental application for XTANDI (enzalutamide) submitted by Astellas.

Competitive
July 19, 2026

Astellas Pharma's ASP5541 Phase 2 Study in Advanced Prostate Cancer Underway

A Phase 2 study is evaluating ASP5541, an injectable form of abiraterone acetate, in men with advanced prostate cancer.

RegulatoryJuly 15, 2026

FDA grants priority review for PADCEV supplemental application

The FDA has accepted a supplemental application for PADCEV (enfortumab vedotin-ejfv) from Astellas, granting it priority review status.

RegulatoryJuly 11, 2026

FDA Approves PADCEV plus Keytruda for Muscle-Invasive Bladder Cancer Treatment

The FDA has approved PADCEV in combination with Keytruda as a neoadjuvant and adjuvant treatment for muscle-invasive bladder cancer, regardless of cisplatin eligibility.

Upcoming milestones

No catalysts indexed for this entity yet.

Related catalysts

No catalysts indexed for this entity yet.

Indications

Bladder Cancer →
Prostate Cancer →

Therapeutic areas

ADC →
Androgen Receptor Inhibitor →
Bladder Cancer →
Hormonal Therapy →
Oncology →
Prostate Cancer →

Newsletter

Get signals before the market moves

Concise strategic intelligence on regulatory, clinical, competitive, and market developments — free to subscribe.

No paywall. No spam. Unsubscribe anytime.