Trial Purpose

Inhloso yalolu cwaningo ukuqhathanisa i-sacituzumab tirumotecan njenge-ejenti eyodwa, futhi ngokuhambisana ne-pembrolizumab, ngokumelene ne-Treatment of Physician’s Choice (TPC) kubahlanganyeli abane-hormone receptor positive/human epidermal growth factor receptor-2 negative (HR+/HER2-) engabukeki endaweni, umdlavuza webele othuthukile, noma i-metastatic.

Ama-hypotheses ayinhloko ukuthi i-sacituzumab tirumotecan njenge-ejenti eyodwa kanye ne-sacituzumab tirumotecan plus pembrolizumab ziphakeme kune-TPC ngokuphathelene nokusinda kwe-progression-free (PFS) Ngokwemibandela Yokuhlola Ukusabela ku-Solid Tumors inguqulo 1.1 (RECIST 1.1 iphuphuthekiswe i-BICR eyingxenye yonke isibuyekezo)

View full trial information on Clinicaltrials.gov

NATIONAL TRIAL REFERENCE NUMBER

I-NCT06312176

EU CT Number

2023-504918-29-00

When speaking to your doctor or clinical trial representative, please have the trial reference number available.

Eligibility

Age Range Icon

Age Range

18+

Sex Icon

Sex

KONKE

About The Study

Trial phase Icon Trial Phase
Trial start Icon Trial start and end dates
  • Actual study start date Ephreli 14, 2024
  • Estimated primary completion date Julayi 11, 2027
  • Estimated study completion date Ephreli 12, 2031

Trial locations

What can you do next?

NATIONAL TRIAL REFERENCE NUMBER

I-NCT06312176

EU CT Number

2023-504918-29-00

When speaking to your doctor or clinical trial representative, please have the trial reference number available.

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