Head-to-head evidence

ICP-490 vs Thalidomide

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.

Multiple Myeloma

Shared mechanism: Cereblon E3 ubiquitin-ligase · full Multiple Myeloma pipeline

ICP-490

Developed by Beijing InnoCare Pharma Tech Co.

Phase 1/2 in Multiple Myelomasmall molecule (cereblon-based molecular glue / IKZF1-3 degrader, CELMoD)
Weak signal

NCT05719701 · Phase 1/2 · status unknown

This is an unblinded, non-randomized dose-finding study with no control arm, and no results have been posted yet, so it cannot currently demonstrate a controlled treatment effect.

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Thalidomide

Marketed by Bristol-Myers Squibb

Approved in Multiple Myelomasmall molecule (IMiD / cereblon modulator, first-generation)
Partial signal

NCT00083551 · Phase 3 · completed

The trial randomly assigned 323 participants to thalidomide and 345 to no thalidomide, but treatment was open-label rather than blinded. Its primary endpoint was the hard clinical outcome of six-year overall survival; although the reported percentages favored thalidomide, statistical significance cannot be determined from the posted registry data.

Next expected readout: August 2027 · NCT00572169 (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: ICP-490's landscape · Thalidomide's landscape