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RECRUITING Phase 1

A Study to Evaluate ALN-BCAT in Patients With Hepatocellular Carcinoma

NCT06600321 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of the dose escalation part of the study is to characterize the safety and tolerability of ALN-BCAT as monotherapy and in combination with pembrolizumab; and to determine the recommended dose(s) for expansion (RDFE) of ALN-BCAT as monotherapy and in combination with pembrolizumab. The purpose of the dose expansion part of the of the study is to evaluate the antitumor activity of ALN-BCAT as monotherapy and in combination with pembrolizumab; to characterize the safety and tolerability of ALN-BCAT as monotherapy and in combination with pembrolizumab.

Interventions

  • DRUG Pembrolizumab
  • DRUG ALN-BCAT

Study Locations (20)

Other

  • Clinical Trial Site — Milan
  • Clinical Trial Site — Rozzano
  • Clinical Trial Site — Verona
  • Clinical Trial Site — Busan

Texas

  • Clinical Trial Site — Dallas
  • Clinical Trial Site — Houston
  • Clinical Trial Site — San Antonio

California

  • Clinical Trial Site — La Jolla
  • Clinical Trial Site — Los Angeles

New York

  • Clinical Trial Site — New York
  • Clinical Trial Site — New York

Arizona

  • Clinical Trial Site — Phoenix

Florida

  • Clinical Trial Site — Jacksonville

Georgia

  • Clinical Trial Site — Atlanta

Illinois

  • Clinical Trial Site — Chicago

Trial Details

FieldValue
Enrollment Target 158 participants
Start Date 2024-12-30
Est. Completion 2027-10-31
Phase Phase 1

Sponsor

Alnylam Pharmaceuticals

81 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06600321

The ClinicalTrials.gov registry entry for NCT06600321 describes a study currently listed as recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 158 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Alnylam Pharmaceuticals, which has 81 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Advanced Hepatocellular Carcinoma appearing as the primary indexed condition, and to 2 interventions — of which Pembrolizumab is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06600321 reports 20 study locations spanning 13 distinct geographic areas — top geographies include Other, Texas, California. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06600321 about?

NCT06600321 is a clinical study titled "A Study to Evaluate ALN-BCAT in Patients With Hepatocellular Carcinoma". The purpose of the dose escalation part of the study is to characterize the safety and tolerability of ALN-BCAT as monotherapy and in combination with pembrolizumab; and to determine the recommended dose(s) for expansion (RDFE) of ALN-BCAT as monotherapy and in combination with pembrolizumab. The pu...

What is the current status of trial NCT06600321?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 158 participants. The study started on 2024-12-30. Estimated completion is 2027-10-31.

What conditions does trial NCT06600321 study?

This clinical trial studies the following conditions: Advanced Hepatocellular Carcinoma, Metastatic Hepatocellular Carcinoma. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06600321?

The interventions under investigation include: Pembrolizumab (DRUG), ALN-BCAT (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06600321?

This trial is sponsored by Alnylam Pharmaceuticals, which has 81 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06600321 being conducted?

This trial has 20 study locations across Arizona, California, Florida, Georgia, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial