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NCT Number: NCT06332430

Intratumoral CAN2109 in Subjects With Solid Tumors

A phase 1, dose escalation, open-label study of intratumoral CAN2109 in subjects with unstable or metastatic advanced solid tumors or lymphomas.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Sun Yat-Sen University Sun Yat-Sen Memorial Hospital

Guangzhou, Guangdong, 510535, China

Location status: Recruiting

Location contact

Herui Yao, Professor

CONTACT

About this study

The scope of the study is to evaluate the safety of CAN2109 in humans, explore its safety, efficacy and collect data on the pharmacokinetics, as well as on the pharmacodynamic effect of the drug on the immune system locally and systemically, and on tumor markers.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Able and willing to provide written informed consent and willing to comply with the study's requirements.
  • Male or female age ≥ 18 years at screening.
  • Metastatic or locally advanced solid tumor that has progressed on, is refractory to, or for which there is no efficacious standard of care therapy. Preferred tumor types include the following:

a. Carcinoma of skin, melanoma, Merkel cell carcinoma (MCC), breast cancer, head and neck squamous cell carcinoma (HNSCC), sarcoma, cervical carcinoma, and colorectal cancer

  • Performance status of 0-1 on the ECOG Performance Scale.

Exclusion criteria

  • Unresolved toxicities from prior therapy, defined as having not resolved to Common Terminology Criteria for Adverse Events (CTCAE) Version 5.0 (v5.0) Grade 0 or 1, with exception of endocrinopathies from prior therapy, alopecia, and vitiligo.
  • Treatment with systemic corticosteroids at doses exceeding 10 mg/day prednisone or equivalent.
  • Has an active infection requiring systemic therapy.
  • Unstable/inadequate cardiac function defined as follows:
  • New York Heart Association Class 3 or 4 congestive heart failure
  • uncontrolled hypertension
  • acute coronary syndrome within 6 months
  • clinical important cardiac arrhythmia
  • mean corrected QT (QTc) interval corrected for heart rate > 480 ms.
  • A history of interstitial lung disease.
  • A history of coagulopathy resulting in uncontrolled bleeding or other bleeding disorders.
  • Participated in a clinical study of an investigational agent within 30 days of screening.
  • Has known psychiatric, substance abuse, or other disorders that would interfere with cooperation with the requirements of the study in the opinion of the investigator.
  • Is pregnant or breastfeeding.

Treatment and study plan

CAN2109

Drug

CAN2109 IT injection (once every 3 weeks)

Primary outcomes

  1. Safety

    Time frame: 12 months

    determined by assessment of dose limiting toxicities per protocol of CAN2109 with cancers.

  2. Recommended Phase 2 Dose (RP2D)

    Time frame: 12 months

    To determine a recommended phase 2 dose of CAN21909 for further development by evaluating number of patients with treatment-related adverse events as assessed by the Common Terminology Criteria for Adverse Events version 5.0 (CTCAE v5.0).

  3. tolerability

    Time frame: 12 months

    determined by assessment of the maximum tolerated dose or maximal assessed dose per protocol of CAN2109 with cancers.

Secondary outcomes

  1. To determine the efficacy of CAN2109

    Time frame: 12 months

    Proportion of patients experiencing a tumor response or a stable disease according to RECIST 1.1 or iRECIST 1.1 as appropriate.

  2. To evaluate the pharmacodynamics of CAN2109

    Time frame: 12 months

    Maximum observed plasma and tumor concentration of CAN2109 after IT administration.

Study contacts

Contact information is provided by the study sponsor or research team.

Erwei Song, MD

CONTACT

[email protected]

+86 020 81332507

Herui Yao, MD

CONTACT

[email protected]

+86 020-34070412

Sponsors and collaborators

Lead sponsor

Canwell Biotech Limited

Industry

Registry information

Official study title

A Phase 1, Dose Escalation, Open-Label Study of Intratumoral CAN2109 in Subjects With Unresectable or Metastatic Advanced Solid Tumors.

Important dates

Study start
2024
Primary completion
2025
Study completion
2026
First posted
Mar 27, 2024
Registry last updated
Dec 19, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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