Company profile
Telix Pharmaceuticals Limited logo

Telix Pharmaceuticals Limited

Pipeline14 assets

  • 177Lu rosopatamab tetraxetanTLX591-Tx / PSMA / Antibody / Urologic Oncology
    Prostate Cancer
  • 177Lu-DOTA-PSMATLX597-Tx / PSMA / Small molecule / Urologic Oncology
    Prostate Cancer
  • 177Lu-girentuximabTLX250-Tx / CAIX / Antibody / Urologic Oncology
    Kidney Cancer / ccRCC
  • 131I-IPATLX101-Tx / LAT / Small molecule / Neuro-oncology
    Brain Cancer / Glioma
  • 90Y-besilesomabTLX66-Tx / CD66 / Antibody / Hematology
    Bone-marrow conditioning
  • 225Ac-RADmAbTLX592-Tx / PSMA / Antibody / Urologic Oncology
    Prostate Cancer
  • 225Ac-girentuximabTLX252-Tx / CAIX / Antibody / Urologic Oncology
    Kidney Cancer
  • UndisclosedTLX400-Tx / FAP / Small molecule / Urologic Oncology
    Bladder Cancer
  • 211At-APATLX102-Tx / LAT / Small molecule / Neuro-oncology
    Brain Cancer
  • -olaratumab conjugateTLX300-Tx / PDGFRα / Antibody / Musculoskeletal Oncology
    Soft Tissue Sarcoma
  • 153Sm-DOTMPTLX090-Tx / Small molecule / Musculoskeletal Oncology
    Bone metastasesPain palliation
  • 68Ga-PSMA-11TLX591-CDx / Illuccix / Gozellix / PSMA / Diagnostic Radiopharmaceutical / Oncology
    Prostate Cancer Imaging
  • 18F-floretyrosineTLX101-CDx / Pixclara / Pixlumi / LAT / Diagnostic Radiopharmaceutical / Neuro-oncology
    Glioma Imaging
  • 89Zr-DFO-girentuximabTLX250-CDx / Zircaix / CAIX / Diagnostic Radiopharmaceutical / Oncology
    Clear Cell Renal Cell Carcinoma (ccRCC) Imaging

Latest news25 items

All news

First Patients Dosed in OPTIMAL-e Trial for Earlier Stage Prostate Cancer

First patients dosed in OPTIMAL-e 1 Phase 2 study evaluating TLX597-Tx for metastatic hormone-sensitive prostate cancer at St Vincent’s Hospital Sydney. OPTIMAL-e will evaluate TLX597-Tx in earlier prostate cancer treatment setting, building on the OPTIMAL-PSMA 2 study which recently completed

Trial Start • Phase 2Trial initiation Wed, Jul 15, 2026

Telix and United Imaging Announce Strategic Theranostics Collaboration

Partnership to evaluate Telix’s innovative precision medicine products and candidates in combination with United Imaging’s advanced scanner platforms. Initial focus on TLX101-Px (Pixclara® 1, Floretyrosine F 18) in the U.S. Framework to support potential co-development, validation, and deployment

ProstACT Global Phase 3 (Part 1) Data Presented in Late-Breaking Oral Session at ASCO 2026

Telix’s first-in-class lutetium radio antibody-drug conjugate (rADC) candidate, TLX591-Tx, demonstrates acceptable tolerability across all standard-of-care (SoC) combination cohorts, with no new safety signals. Findings support feasibility of TLX591-Tx in combination with contemporary SoC in

Presentation / Abstract • Phase 3ASCO late-breaking oral presentation Mon, Jun 1, 2026
Telix Pharmaceuticals Limited • Endpoint Arena