Working…
ClinicalTrials.gov
ClinicalTrials.gov Menu

Gleolan for Visualization of Newly Diagnosed or Recurrent Meningioma (MEN-301)

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. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT04305470
Recruitment Status : Recruiting
First Posted : March 12, 2020
Last Update Posted : July 16, 2021
Sponsor:
Information provided by (Responsible Party):
NX Development Corp

Brief Summary:
This Phase 3 open-label single-arm study is designed to investigate the safety, diagnostic performance, and clinical usefulness of Gleolan for the real time detection and visualization of meningiomas during tumor resection surgery. The study is planned to run for 15 months with individual study participation lasting for approximately 2 months.

Condition or disease Intervention/treatment Phase
Meningioma Drug: Gleolan (Aminolevulinic Acid Hydrochloride/ALA/ALA-HCI) Phase 3

Detailed Description:

This Phase 3 open-label single-arm study is designed to investigate the safety, diagnostic performance, and clinical usefulness of the imaging agent Gleolan™ (Aminolevulinic Acid Hydrochloride, ALA HCl, ALA, 5-ALA), an orally administered imaging agent for the real time detection and visualization of meningiomas during tumor resection surgery. ALA is a prodrug that is metabolized intracellularly to form the fluorescent molecule Protoporphyrin IX (PpIX). The exogenous application of ALA leads to a highly selective accumulation of PpIX in tumor cells. Following excitation with blue light (BL) (λ = 375 - 440 nm), the PpIX, which has accumulated selectively in tumor tissue, emits a red-violet light. This phenomenon allows for the real-time visualization of tumor tissue during resection surgery.

Patients about to undergo resection for suspected meningioma [World Health Organization (WHO) Grade I, II, III] will be screened and informed consent will be obtained prior to surgery and prior to study participation. Eligible study participants will receive an oral solution of Gleolan (20 mg/kg body weight) 3 hours, (target range 2-4 hours) prior to anesthesia, and then undergo surgery for meningioma resection. During the surgery, the surgeon will use a microscope equipped with WL and BL for visualization of Gleolan-induced PpIX fluorescence for the selection of protocol-driven tissue locations and to assess fluorescence status.

Study participants will be evaluated within 48 hours post procedure, 2 weeks post procedure, and 6 weeks post procedure for study safety assessment.

Layout table for study information
Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 100 participants
Allocation: N/A
Intervention Model: Single Group Assignment
Intervention Model Description: Phase 3, open-label, single arm study.
Masking: None (Open Label)
Primary Purpose: Diagnostic
Official Title: A Phase 3 Multicenter Study of Gleolan (Aminolevulinic Acid Hydrochloride) to Enhance Visualization of Tumor in Patients With Newly Diagnosed or Recurrent Meningiomas
Actual Study Start Date : October 28, 2020
Estimated Primary Completion Date : January 1, 2022
Estimated Study Completion Date : January 1, 2022


Arm Intervention/treatment
Experimental: Single Arm
Open-label, single-arm
Drug: Gleolan (Aminolevulinic Acid Hydrochloride/ALA/ALA-HCI)
One time oral dose on day of surgery (20 mg/kg bodyweight)




Primary Outcome Measures :
  1. The proportion of participants who have at least one indeterminate tissue or unexpected fluorescent End of Surgery (EOS) tissue where Gleolan-induced PpIX fluorescence status is consistent with histology. [ Time Frame: Surgery (Day 1) ]
    Per Protocol Population


Secondary Outcome Measures :
  1. Positive Predicted Value (PPV) of Gleolan-induced PpIX fluorescence of the single bulk tumor tissue obtained from each study participant [ Time Frame: Surgery (Day 1) ]
    Per Protocol Population

  2. Diagnostic accuracy of Gleolan-induced PpIX fluorescence among indeterminate tissue and unexpected fluorescent EOS tissue locations is at least 20% greater than the diagnostic accuracy of the surgeons' assessment. [ Time Frame: Surgery (Day 1) ]
    Biopsy Efficacy Analysis Population

  3. Diagnostic performance of Gleolan-induced PpIX fluorescence will be computed for indeterminate tissue biopsies, unexpected fluorescent EOS tissue biopsies. [ Time Frame: Surgery (Day 1) ]
    Biopsy Efficacy Analysis Population

  4. The concordance between the Surgeon and Adjudication Panel assessment of white light (WL) visualization visualization to identify tissue as likely or unlikely to be meningioma among indeterminate tissues. [ Time Frame: Surgery (Day 1) ]
    Biopsy Efficacy Analysis Population

  5. The concordance between the Surgeon and Adjudication Panel assessment of blue light (BL) visualization to identify fluorescence status of indeterminate tissues. [ Time Frame: Surgery (Day 1) ]
    Biopsy Efficacy Analysis Population



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.


Layout table for eligibility information
Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. A pre-operative MRI within ≥ 90 days of study enrollment documenting a suspected meningioma or suspected recurrence of a meningioma for which a complete meningioma resection is indicated and has been planned.
  2. Adult age ≥ 18 years.
  3. Patient must have normal organ and bone marrow function and be appropriate surgical candidates per site SOC.
  4. Patient must have recording of each parameter as defined below:

    Bilirubin Below upper limit of normal AST (SGOT) < 2.5 X institutional upper limit of normal ALT (SGPT) < 2.5 X institutional upper limit of normal Creatinine Below upper limit of normal OR Creatinine clearance >60 mL/min/1.73 m2 for participants with creatinine levels above institutional normal

  5. The patient must demonstrate the ability to understand the informed consent document and the willingness and ability to sign a written informed consent document. The study consent documents will be prepared in English and German and Spanish. Translation for non-English, non-German, or non-Spanish speaking participants will be provided as appropriate by institution, as required.
  6. WOCBP and men participating must agree to use highly effective forms of contraception, and men must also agree not to donate sperm for the duration of treatment, and for at least 42 days after the one time use of the study drug.

Exclusion Criteria:

  1. History of allergic reactions attributed to compounds of similar chemical/biologic composition to Gleolan.
  2. Known or documented personal or family history of porphyria.
  3. Uncontrolled concurrent illness, including but not limited to ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia or psychiatric illness.
  4. Patient has had a meningioma resection or radiation treatment within 90 days of informed consent.
  5. Social or medical situations that would limit compliance with study requirements (e.g. ability to travel for follow-up or inability to obtain appropriate pre-op MRI (e.g. cardiac pacemaker).
  6. Women who are pregnant or plan to become pregnant during study participation.
  7. Prior history of gastrointestinal perforation, diverticulitis, and or/peptic ulcer disease.
  8. Simultaneous participation in another clinical study or participation in another clinical study in the 30 days directly preceding treatment or within 5 plasma half-life of the preceding study drug, whatever is longer.
  9. Simultaneous use of other potentially phototoxic substances (St. John's wort, griseofulvin, thiazide diuretics, sulfonylureas, phenothiazines, sulphonamides, quinolones and tetracyclines), and topical preparations containing ALA for 24 hours during the perioperative period (see MOPS for detailed list).
  10. Unwillingness by patient to sign consent or return for subsequent visits following surgery.
  11. Any condition that in the opinion of the Investigator would exclude the patient as a viable candidate for this study.

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 ClinicalTrials.gov identifier (NCT number): NCT04305470


Contacts
Layout table for location contacts
Contact: Ashley Cox, MBA, CCRP 502-316-8981 acox@nxdevcorp.com
Contact: Kelly Sims, CRN, SCRN 267-977-7870 ksims@nxdevcorp.com

Locations
Layout table for location information
United States, Arizona
Mayo Clinic Recruiting
Phoenix, Arizona, United States, 85054
Contact: Evelyn Turcotte       turcotte.evelyn@mayo.edu   
Principal Investigator: Bernard Bendok, MD         
United States, California
University of California San Diego Not yet recruiting
La Jolla, California, United States, 92093
Contact: Marc Schwartz, MD         
Principal Investigator: Marc Schwartz, MD         
Keck Hospital of USC Recruiting
Los Angeles, California, United States, 90033
Contact: Trey Garrett       normanga@usc.edu   
Principal Investigator: Gabriel Zada, MD         
Providence St. Joseph Hospital Recruiting
Orange, California, United States, 92868
Contact: Lillian Chen       lillian.chen@stjoe.org   
Contact: Joscelyn Green       joscelyn.green@stjoe.org   
Principal Investigator: Lars Anker, MD         
United States, Florida
Baptist Health South Florida Not yet recruiting
Miami, Florida, United States, 33176
Principal Investigator: Michael McDermott, MD         
United States, Illinois
Southern Illinois University Medicine Not yet recruiting
Springfield, Illinois, United States, 62794
Contact: Barbara Lokaitis       blokaitis@siumed.edu   
Principal Investigator: Jeffrey Cozzens, MD         
United States, Massachusetts
Massachusetts General Hospital Not yet recruiting
Boston, Massachusetts, United States, 02114
Contact: Akeive Burrows       ajburrows@mgh.harvard.edu   
Principal Investigator: Bob Carter, MD         
United States, Michigan
Henry Ford Health System Recruiting
Detroit, Michigan, United States, 48202
Contact: Lisa Scarpace       lscarpa1@hfhs.org   
Contact: Lisa         
Principal Investigator: Adam Robin, MD         
United States, Minnesota
Mayo Clinic Rochester Recruiting
Rochester, Minnesota, United States, 55905
Contact: Yeoniee Kim       Kim.yeoniee@mayo.edu   
Principal Investigator: Jaime Van Gompel, MD         
United States, New York
NYU Langone Health Recruiting
Brooklyn, New York, United States, 11220
Contact: Cathryn Lapierre       cathryn.lapierre@nyulangone.org   
Principal Investigator: John Golfinos, MD         
Sub-Investigator: Donato Pacione, MD         
Weill Cornell Medicine Not yet recruiting
New York, New York, United States, 10065
Contact: Theodore Schwartz, MD         
Principal Investigator: Theodore Schwartz, MD         
United States, Pennsylvania
University of Pennsylvania- Penn Medicine Not yet recruiting
Philadelphia, Pennsylvania, United States, 19104
Contact: Marie Kerr, CCRP       marie.kerr@pennmedicine.upenn.edu   
Principal Investigator: John Lee, MD         
UPMC Recruiting
Pittsburgh, Pennsylvania, United States, 15213
Contact: Benita Valappil       valappilb2@upmc.edu   
Principal Investigator: Paul Gardner, MD         
Sub-Investigator: Georgios Zenonos, MD         
United States, Texas
MD Anderson Recruiting
Houston, Texas, United States, 77030
Contact: Summer Stovall         
Principal Investigator: Shaan Raza, MD         
Sub-Investigator: Jeffrey Weinberg, MD         
Austria
Medical University of Vienna Recruiting
Vienna, Austria, 1090
Contact: Georg Widhalm, MD       georg.widhalm@meduniwien.ac.at   
Contact: Julia Freund       julia.freund@meduniwien.ac.at   
Principal Investigator: Georg Widhalm, MD         
Germany
University Hospital Münster Recruiting
Münster, Germany
Contact: Walter Stummer, MD       walter.stummer@ukmuenster.de   
Sponsors and Collaborators
NX Development Corp
Investigators
Layout table for investigator information
Principal Investigator: Walter Stummer, MD Universitätsklinikum Münster
Principal Investigator: Bernard Bendok, MD Mayo Clinic
Layout table for additonal information
Responsible Party: NX Development Corp
ClinicalTrials.gov Identifier: NCT04305470    
Other Study ID Numbers: NXDC-MEN-301
First Posted: March 12, 2020    Key Record Dates
Last Update Posted: July 16, 2021
Last Verified: July 2021

Layout table for additional information
Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by NX Development Corp:
ALA
fluorescence guided surgery
Gleolan
meningioma
Additional relevant MeSH terms:
Layout table for MeSH terms
Meningioma
Neoplasms, Nerve Tissue
Neoplasms by Histologic Type
Neoplasms
Neoplasms, Vascular Tissue
Meningeal Neoplasms
Central Nervous System Neoplasms
Nervous System Neoplasms
Neoplasms by Site
Nervous System Diseases
Aminolevulinic Acid
Photosensitizing Agents
Dermatologic Agents