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REGNRegeneron PharmaceuticalsSigning up patients

Study of REGN4018 (Ubamatamab) Administered Alone or in Combination With Cemiplimab in Adult Patients With Recurrent Ovarian Cancer or Other Recurrent Mucin-16 Expressing (MUC16+) Cancers

Recurrent Ovarian Cancer · Recurrent Fallopian Tube Cancer · Recurrent Primary Peritoneal Cancer · Recurrent Endometrial Cancer · Endometrial Cancer · Low-grade Serous Ovarian Cancer

5Calmworry score, out of 100

No strong warning signs right now. The score counts warning signs; it is not a prediction.

Why this score

  • 5 insiders sold shares within a month

    Since Nov 4, 2026 · was worth 5, fading over time

    +4.8
Worry score5

Score over time

Stage
Phase 1/2
Patients
890 (planned)
Started
May 21, 2018
Main results expected
May 10, 2027
Fully finished
May 10, 2027
Results posted
not yet

What counts as success

The trial's main goal(s), called the “primary outcome.”

  • Number of participants with Dose-limiting toxicity (DLTs) for ubamatamab monotherapy

    Measured over: From Cycle 1, Day 1 up to 35 days

  • Number of participants with DLTs for ubamatamab with cemiplimab

    Measured over: From Cycle 2, Day 1 up to 21 days

  • Number of participants with Treatment-emergent adverse event (TEAE)s (including immune-related adverse events (imAEs)) for ubamatamab monotherapy

    Measured over: Up to 2 years

  • Number of participants with TEAEs (including imAEs) for ubamatamab with cemiplimab

    Measured over: Up to 2 years

  • Number of participants with serious adverse events (SAEs) for ubamatamab monotherapy

    Measured over: Up to 2 years

  • Number of participants with SAEs for ubamatamab with cemiplimab

    Measured over: Up to 2 years

  • Number of deaths for ubamatamab monotherapy

    Measured over: Up to 2 years

  • Number of deaths for ubamatamab with cemiplimab

    Measured over: Up to 2 years

  • Number of participants with laboratory abnormalities (grade 3 or higher per Common Terminology Criteria for Adverse Events [CTCAE]) for ubamatamab monotherapy

    Measured over: Up to 2 years

  • Number of participants with laboratory abnormalities (grade 3 or higher per CTCAE) for ubamatamab with cemiplimab

    Measured over: Up to 2 years

  • Concentration of ubamatamab in serum over time for ubamatamab monotherapy

    Measured over: Up to 2 years

Changes Tremor has spotted

No changes since Tremor started watching this trial.
Show details (technical version)

Score inputs

  • insider_selling_cluster: base 5, now 4.8, since 2026-11-04, fades (half-life)

Raw record changes

  • none yet

Trial ID NCT03564340 · record last updated 2026-09-25 · checked 2026-11-09 15:47 UTC

See the official record on ClinicalTrials.gov (NCT03564340) ↗
  • Concentration of ubamatamab in serum over time for ubamatamab with cemiplimab

    Measured over: Up to 2 years

  • Objective response rate (ORR) defined by Response Evaluation Criteria in Solid Tumors (RECIST 1.1) for ubamatamab monotherapy

    Measured over: Up to 2 years

  • ORR defined by RECIST 1.1 for ubamatamab with cemiplimab

    Measured over: Up to 2 years