Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT03861793 · ClinicalTrials.gov registry record · Phase 1

A Dose Escalation and Cohort Expansion Study of Subcutaneously-Administered Cytokine ALKS 4230 (Nemvaleukin Alfa) as a Single Agent and in Combination With Anti-PD-1 Antibody (Pembrolizumab) in Subjects With Select Advanced or Metastatic Solid Tumors (ARTISTRY-2)

A Phase 1 study, sponsored by Mural Oncology.

Completed
Registry status
Phase 1
Development phase
116
Enrollment target

NCT03861793: Completed Phase 1 study, sponsored by Mural Oncology.

NCT03861793 is a Phase 1 study that has completed, run by Mural Oncology. The registered enrollment target is 116 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (93% higher). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT03861793, a Phase 1 study, has completed, sponsored by Mural Oncology.

COMPLETED
Registry status
Phase 1
Development phase
116 participants
Enrollment target

Study Summary

This study will characterize the safety and tolerability and identify the recommended Phase 2 dose (RP2D) of subcutaneous (SC) ALKS 4230 as monotherapy and in combination with pembrolizumab.

Primary Outcome

Includes AEs that are both serious and drug-related

Interventions

  • BIOLOGICAL Pembrolizumab
  • BIOLOGICAL ALKS 4230

Trial Details

FieldValue
Enrollment Target 116 participants
Start Date 2019-02-26
Est. Completion 2023-03-01
Phase Phase 1
Mural Oncology

6 total trials

What the finished NCT03861793 record still lists

NCT03861793 is an interventional study that assigns participants to a tested intervention. The registered 116 participants enrollment target is mid-sized for trials with a published cap, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (93% higher).

The record links to 0 conditions, and to 2 interventions - of which Pembrolizumab is the first listed.

NCT03861793 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03861793 about?

NCT03861793 is a clinical study titled "A Dose Escalation and Cohort Expansion Study of Subcutaneously-Administered Cytokine ALKS 4230 (Nemvaleukin Alfa) as a Single Agent and in Combination With Anti-PD-1 Antibody (Pembrolizumab) in Subjects With Select Advanced or Metastatic Solid Tumors (ARTISTRY-2)". This study will characterize the safety and tolerability and identify the recommended Phase 2 dose (RP2D) of subcutaneous (SC) ALKS 4230 as monotherapy and in combination with pembrolizumab.

What is the current status of trial NCT03861793?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 116 participants. The study started on 2019-02-26. Estimated completion is 2023-03-01.

What interventions are being tested in trial NCT03861793?

The interventions under investigation include: Pembrolizumab (BIOLOGICAL), ALKS 4230 (BIOLOGICAL).

Who is sponsoring clinical trial NCT03861793?

This trial is sponsored by Mural Oncology, which has 6 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03861793's enrollment target sits among peer trials

116 501st of 2000 higher than 1,497 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT03014687 · 116 participants · Phase 4

    Prophylactic Oral Antibiotics on Sinonasal Outcomes Following Endoscopic Transsphenoidal Surgery for Pituitary Lesions

  • NCT03214562 · 116 participants · Phase 1

    Venetoclax With Combination Chemotherapy in Treating Patients With Newly Diagnosed or Relapsed or Refractory Acute Myeloid Leukemia

  • NCT03847467 · 116 participants · Phase 1

    Pilot and Feasibility Study of 2'-FL as a Dietary Supplement in IBD Patients Receiving Stable Maintenance Anti-TNF Therapy

  • NCT04222413 · 116 participants · Phase 1

    Metarrestin (ML-246) in Subjects With Metastatic Solid Tumors

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT03861793, the US trial registry maintained by the National Library of Medicine. NCT03861793 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.