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Completed

NCT Number: NCT03015883

Alpha Radiation Emitters Device for the Treatment of Squamous Cell Carcinoma

A unique approach for cancer treatment employing intratumoral diffusing alpha radiation emitter device.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Davidof Cancer Institution at the Rabin Medical Center Israel

Petah Tikva, 49100, Israel

About this study

This will be a prospective, first in man, controlled study, assessing the safety and efficacy of diffusing alpha emitters radiation therapy (DaRT) delivered through radioactive seeds inserted into the tumor.

This approach combines the advantages of local intratumoral irradiation of the tumor, as used in conventional brachytherapy, with the power of the alpha radiation emitting atoms, that will be introduced in quantities considerably lower than radiation therapy already used in patients.

Lesions with histopathological diagnosis of squamous cell carcinoma will be studied.

Reduction in tumor size 30 days after DaRT insertion will be assessed.

Safety will be assessed by the incidence, severity and frequency of all Adverse Events (AE).

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Histopathological confirmation of squamous cell carcinoma.
  • Tumor size ≤ 5 centimeters in the longest diameter.
  • Age over 18.
  • Women of childbearing potential will have evidence of negative pregnancy test.
  • Life expectancy of more than 6 months.
  • Performance status 2 (ECOG scale) or less.
  • Signed informed consent form.

Exclusion criteria

  • Tumor maximal diameter > 5 centimeters.
  • Tumor of Keratoacanthoma histology.
  • Performance status ≥ 3 (ECOG scale).
  • Patients with moribund diseases, autoimmune diseases or vasculitis.
  • Patients under immunosuppressive and/or corticosteroid treatment.
  • Volunteers that participated in other studies in the past 30 days.

Treatment and study plan

Diffusing Alpha Radiation Emitters Therapy (DaRT)

Radiation

An intratumoral insertion of a seed(s), loaded with Radium-224, securely fixed in the seeds. The seeds release by recoil into the tumor short-lived alpha-emitting atoms.

Other names: DaRT

Primary outcomes

  1. Adverse Events

    Time frame: 30-45 days post seed insertion

    The incidence, severity and frequency of all Adverse Events

  2. Reduction in Tumor size

    Time frame: 30-45 days post seed insertion

    The reduction in tumor size 30-45 days after DaRT insertion

Secondary outcomes

  1. Percent of NecroticTissue

    Time frame: 30-45 days post seed insertion

    Percent of necrotic tissue in the tumor 30 days after DaRT insertion

Sponsors and collaborators

Lead sponsor

Alpha Tau Medical LTD.

Industry

Registry information

Official study title

A Safety and Effectiveness Study of Intratumoral Diffusing Alpha Radiation Emitters on Squamous Cell Carcinoma (First in Man)

Acronym: DaRT

Important dates

Study start
2017
Primary completion
2019
Study completion
2019
First posted
Jan 10, 2017
Registry last updated
Jan 13, 2021

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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