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Fluorescence-guided Resection in Breast Cancer

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT01110954
Recruitment Status : Terminated (Insufficient recruitment)
First Posted : April 27, 2010
Last Update Posted : April 4, 2017
Information provided by (Responsible Party):
photonamic GmbH & Co. KG

Brief Summary:
This is an explorative phase II study to investigate the suitability of PD L 506 in the specific intra-operative detection of breast tumour tissue.

Condition or disease Intervention/treatment Phase
Breast Tumour Drug: PD L 506 Phase 2

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 8 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Triple (Participant, Investigator, Outcomes Assessor)
Primary Purpose: Diagnostic
Official Title: Evaluation of the Suitability of PD L 506 for Intraoperative Visualisation of Palpable and Nonpalpable Breast Cancer Tissue
Actual Study Start Date : May 31, 2010
Actual Primary Completion Date : July 19, 2012
Actual Study Completion Date : December 20, 2012

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Breast Cancer

Arm Intervention/treatment
Active Comparator: PD L 506 2nd dose
Different dosage
Drug: PD L 506
Two different doses will be compared

Experimental: PD L 506 Drug: PD L 506
Two different doses will be compared

Primary Outcome Measures :
  1. Fluorescence intensity in breast cancer tissue [ Time Frame: 3 h after intake of study medication ]

Secondary Outcome Measures :
  1. Laboratory data and adverse events [ Time Frame: 14 days ]

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Written informed consent
  • Caucasian female postmenopausal patients
  • Patients with histologically confirmed primary palpable and nonpalpable breast cancer sized up to 5 cm (T1 - T2)

Exclusion Criteria:

  • Suspicious lymphogenic metastases (cN1-3)
  • Acute or chronic hepatic diseases
  • Manifest renal diseases with renal dysfunction
  • Relevant cardiac disease
  • Preceding therapy of breast tumour under investigation
  • Patients with multiple attempts of hook-wire placement in preparation of surgery
  • Dementia or psychic condition that might interfere with the ability to understand the study and thus give a written informed consent
  • Simultaneous participation in another clinical study or participation in another clinical study in the 30 days directly preceding treatment

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT01110954

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Munich, Germany
Sponsors and Collaborators
photonamic GmbH & Co. KG

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Responsible Party: photonamic GmbH & Co. KG Identifier: NCT01110954    
Other Study ID Numbers: MK01
First Posted: April 27, 2010    Key Record Dates
Last Update Posted: April 4, 2017
Last Verified: April 2017
Additional relevant MeSH terms:
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Breast Neoplasms
Neoplasms by Site
Breast Diseases
Skin Diseases