Head-to-head evidence

Capivasertib vs NTQ1062

Same mechanism, same race: design-graded trial evidence for both assets, with the grading rationale shown. Grades describe the quality of the evidence, never the merits of either security.

HR+/HER2- Metastatic Breast Cancer

Shared mechanism: AKT (inhibitor) · full HR+/HER2- Metastatic Breast Cancer pipeline

Capivasertib

Marketed by AstraZeneca

Approved in HR+/HER2- Metastatic Breast Cancersmall molecule
Partial signal

NCT01625286 · Phase 1/2 · completed

The trial randomized and quadruple-blinded 148 participants and used placebo plus paclitaxel as the control; the Part B primary endpoint was RECIST-defined progression-free survival in 110 patients. Although progression-free survival numerically favored capivasertib (10.9 versus 8.4 months), the primary comparison was not statistically significant (HR 0.80, p=0.308), so the evidence is moderate rather than strong.

Next expected readout: October 2026 · NCT06635447 (registry estimate)

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NTQ1062

Developed by Sino Biopharmaceutical

Phase 3 in HR+/HER2- Metastatic Breast Cancersmall molecule
not yet graded

No graded featured trial for this indication yet; the grade above reflects that absence, not a judgment.

Next expected readout: August 2028 · NCT07393321 (registry estimate)

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The full competitive landscape for each asset (every same-race competitor with aligned evidence, sortable) is on the asset pages: Capivasertib's landscape · NTQ1062's landscape