Actively Recruiting

Phase 1
Age: 18Years +
All Genders
NCT06504368

Safety, Tolerability, and Pharmacokinetics of DCR-PDL1 in Adults With Solid Tumors

Led by Dicerna Pharmaceuticals, Inc., a Novo Nordisk company · Updated on 2025-11-06

32

Participants Needed

2

Research Sites

187 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The study will evaluate the safety, tolerability, and pharmacokinetics of intravenous DCR-PDL1 in adults with solid tumors. Participants will be enrolled in one of 4 ascending-dose cohorts. Each treatment cycle will consist of multiple intravenous (IV) doses. Dose escalation decisions will be based on data collected during the dose-limiting toxicity (DLT) period.

CONDITIONS

Official Title

Safety, Tolerability, and Pharmacokinetics of DCR-PDL1 in Adults With Solid Tumors

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 years or older
  • Documented locally advanced or metastatic solid tumor malignancy or non-Hodgkin's lymphoma
  • Cancer that is refractory to, progressed after, relapsed after, or intolerant to standard therapy known to benefit their condition, or with no available standard therapy
  • Measurable disease according to RECIST version 1.1
  • Malignancy not suitable for surgical treatment
  • ECOG performance status of 0, 1, or 2
  • Anticipated life expectancy of at least 3 months at consent
  • Other protocol-defined inclusion criteria may apply
Not Eligible

You will not qualify if you...

  • Known central nervous system or leptomeningeal metastases not controlled by prior surgery or radiotherapy
  • Symptoms indicating central nervous system involvement requiring treatment
  • Other protocol-defined exclusion criteria may apply

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

NEXT Oncology

Irving, Texas, United States, 75039

Actively Recruiting

2

Next Oncology

San Antonio, Texas, United States, 78229

Actively Recruiting

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Research Team

N

Novo Nordisk

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SEQUENTIAL

Primary Purpose

TREATMENT

Number of Arms

1

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Safety, Tolerability, and Pharmacokinetics of DCR-PDL1 in Adults With Solid Tumors | DecenTrialz