Head-to-head evidence

CID-103 vs Daratumumab

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: CD38 · full Multiple Myeloma pipeline

CID-103

Developed by CASI Pharmaceuticals, Inc.

Phase 1 in Multiple Myelomamonoclonal antibody (fully human IgG1, anti-CD38)
Weak signal

NCT04758767 · Phase 1 · completed

All participants received CID-103 with no placebo or comparator arm and no blinding, so the design cannot show whether the antibody works better than another option. Registry results were not posted at the time of grading; the key result shown was recovered from the cited external source.

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Daratumumab

Marketed by Johnson & Johnson

Approved in Multiple Myelomamonoclonal antibody
Partial signal

NCT02076009 · Phase 3 · completed

This was a large randomized, open-label trial with an active comparator, enrolling 286 participants in the daratumumab group and 283 in the control group. Progression-free survival was the hard clinical primary endpoint, but the registry does not report a complete treatment comparison or statistical significance for it, so the result cannot be clearly classified as met.

Next expected readout: October 2026 · NCT06140966 (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: CID-103's landscape · Daratumumab's landscape