- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT07733674
Study of 203Pb-RMX-VH-PIB Dosimetry and Biodistribution in Patients With Glioblastoma Multiform (GBM) and Pancreatic Ductal Adenocarcinoma (PDAC) (RMX-VH)
Dosimetry and Bio-distribution of 203Pb-RMX-VH-PIB in Newly Diagnosed or Recurrent Patients With Solid Tumors: A Phase I Exploratory Study
The goal of this Phase I clinical trial is to evaluate how the imaging drug 203Pb- RMX-VH-PIB distributes in the body and how much radiation different organs receive in patients with glioblastoma multiforme (GBM) or pancreatic ductal adenocarcinoma (PDAC).
The main questions it aims to answer are:
How does 203Pb-RMX-VH-PIB spread in the body (biodistribution)? What is the radiation dose delivered to organs (dosimetry)?
Participants will:
Receive a single intravenous (IV) injection of 203Pb-RMX-VH-PIB. Undergo multiple single-photon emission computed tomography/computed tomography (SPECT/CT) imaging scans.
Have blood, urine, vital signs, and electrocardiogram (ECG) monitored for safety.
Be followed for any side effects for up to 30 days.
Studienübersicht
Status
Intervention / Behandlung
Detaillierte Beschreibung
Studientyp
Einschreibung (Geschätzt)
Phase
- Phase 1
Kontakte und Standorte
Studienkontakt
- Name: Ebrahim Delpassand, MD, FACNM
- Telefonnummer: 713-499-9733
- E-Mail: edelpassand@radiomedix.com
Studieren Sie die Kontaktsicherung
- Name: Izabela Tworowska, MSPharm, PhD
- Telefonnummer: 832-868-2812
- E-Mail: itworowska@radiomedix.com
Studienorte
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Texas
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Houston, Texas, Vereinigte Staaten, 77042
- Rekrutierung
- Excel Diagnostics & Nuclear Oncology Center
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Kontakt:
- Susan Cork
- Telefonnummer: 3203 713-781-6200
- E-Mail: scork@exceldiagnostics.com
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Kontakt:
- Nereyda Sauceda Sauceda
- Telefonnummer: 3246 713-781-6200
- E-Mail: nsauceda@exceldiagnostics.com
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Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
- Älterer Erwachsener
Akzeptiert gesunde Freiwillige
Beschreibung
Inclusion Criteria:
- Signed informed consent.
- Subjects aged ≥18 years.
- Karnofsky status ≥60.
- Negative urine pregnancy test in women of childbearing potential.
Histologically confirmed and /or highly suspicious GBM (Adult type Astrocytoma grade IV both IDH-Mutant and IDH-Wild Type) including primary, recurrent or stable enhancing residual or primary, recurrent or stable enhancing residual PDAC.
a. GBM group i. Contrast enhanced Brain MRI image with results compatible with GBM within the 2 weeks of dosing day.
ii. Tumor size of ≥ 1.0 cm in any dimension by MRI. iii. No antiangiogenic therapy within 4 weeks of the day of dosing. iv. No chemotherapy within 2 weeks of the day of dosing. v. Subjects receiving corticosteroids must be on a stable or decreasing dose regimen prior to enrollment b. PDAC group i. No chemotherapy within 2 weeks of the day of dosing ii. Tumor size of ≥ 1.0 cm in any dimension by MRI or CT
Recent blood test results (within 4 weeks pre-dose) as follows:
- WBC: ≥ 2 x 109/L
- Haemoglobin: ≥ 8 g/dL
- Platelets: ≥75 x 109/L
- ALT, AST, AP ≤ 5 times ULN
- Bilirubin: ≤ 2 times ULN
- Creatinine clearance ≥ 60 mL/min, calculated by the Cockcroft-Gault equation
Exclusion Criteria:
- Known hypersensitivity to RMX-VH peptide analogue, 203Pb-RMX-VH-PIB, 203Pb (Lead) , or any of the excipients of 203Pb-RMX-VH-PIB.
- Inability to undergo MRI or CT/SPECT/CT scans
- Current somatic or psychiatric disease/condition that may interfere with consent or the objectives and assessments of the study.
- Pregnancy or plans to conceive during the course of study participation.
- In GBM groups participants requiring MRI: History of hypersensitivity or contraindication to gadolinium-based contrast agents, including prior allergic or anaphylactoid reactions to gadolinium contrast media, or any condition (e.g., severe renal impairment, acute kidney injury) that, in the investigator's judgment, increases the risk associated with gadolinium administration.
- In PDAC groups participants requiring CT scans: Any contraindications to iodinated contrast agents include a history of severe hypersensitivity or allergic reaction to iodinated contrast media, significant renal impairment (e.g., eGFR < 30 mL/min/1.73 m² or acute kidney injury), uncontrolled hyperthyroidism or other thyroid disorders that may worsen with iodine exposure, prior contrast-induced nephropathy, pregnancy, and any unstable medical condition such as severe heart failure or hemodynamic instability that, in the investigator's judgment, increases the risk of contrast administration.
- Male and female participants of childbearing potential who are unwilling or unable to use an acceptable method of contraception for the duration of the study.
- Women who are breastfeeding
- Participants who are currently receiving treatment with statins (HMG-CoA reductase inhibitors), including but not limited to atorvastatin, rosuvastatin, pitavastatin, simvastatin, lovastatin, pravastatin, or fluvastatin, are excluded unless the medication has been discontinued for at least four (4) drug half-lives prior to administration of the investigational product
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Diagnose
- Zuteilung: N / A
- Interventionsmodell: Einzelgruppenzuweisung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
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Experimental: 203Pb-RMX-VH-PIB Imaging
All participants will receive a single intravenous injection of 203Pb-RMX-VH-PIB (5.0 ± 10% mCi).
Following administration, participants will undergo multiple SPECT/CT scans to evaluate the biodistribution and radiation dosimetry of the investigational radiopharmaceutical.
Safety assessments will include monitoring of vital signs, blood exams, and electrocardiograms (ECGs) before and after dosing, with adverse events recorded for up to 30 days.
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A single intravenous (IV) injection of the investigational radiopharmaceutical 203Pb-RMX-VHPIB administered to eligible patients.
Andere Namen:
Serial whole-body and region-specific SPECT/CT scans performed after IP administration to assess biodistribution and dosimetry
Andere Namen:
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Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Whole-body and organ-specific absorbed radiation dose for 203Pb-RMX-VH-PIB
Zeitfenster: From injection to up to 144 hours post-injection, multi-time-point SPECT/CT, approximately 1-2 hours, 4-6 hours, 24 hours, 48 hours, 120 hours, and, if needed, 144 hours after injection.
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Whole-body and organ-specific absorbed radiation doses will be estimated using serial quantitative SPECT/CT imaging and available blood and urine radioactivity data following a single intravenous administration of 203Pb-RMX-VH-PIB.
Absorbed radiation doses will be summarized per unit of administered activity, such as mGy/MBq.
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From injection to up to 144 hours post-injection, multi-time-point SPECT/CT, approximately 1-2 hours, 4-6 hours, 24 hours, 48 hours, 120 hours, and, if needed, 144 hours after injection.
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Organ-Specific Absorbed Dose of 203Pb-RMX-VH-PIB
Zeitfenster: From injection to up to144 hours post-injection, multi-time-point SPECT/CT, approximately 1-2 hours, 4-6 hours, 24 hours, 48 hours, 120 hours, and, if needed, 144 hours after injection.
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For each participant, volumes of interest (VOIs) will be delineated over critical organs, including the kidneys, liver, spleen, red marrow, pancreas, brain, thyroid, and salivary glands, as well as target lesions.
Time-activity curves will be fitted, and residence times will be derived.
The absorbed dose per unit of injected activity will be calculated using the standard Medical Internal Radiation Dose (MIRD) schema with Organ Level Internal Dose Assessment/Exponential Modeling (OLINDA/EXM) software or an equivalent method.
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From injection to up to144 hours post-injection, multi-time-point SPECT/CT, approximately 1-2 hours, 4-6 hours, 24 hours, 48 hours, 120 hours, and, if needed, 144 hours after injection.
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Mitarbeiter und Ermittler
Sponsor
Ermittler
- Studienstuhl: Ebrahim Delpassand, MD, FACNM, Radiomedix, Inc.
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Geschätzt)
Primärer Abschluss (Geschätzt)
Studienabschluss (Geschätzt)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
- Gehirntumor
- bösartiges Gliom
- Bauchspeicheldrüsenkrebs
- hochgradiges Gliom
- bösartiger Hirntumor
- Duktales Adenokarzinom des Pankreas (PDAC)
- Astrozytom
- Radiopharmakon
- Glioblastoma multiforme (GBM)
- diagnostisches Radiopharmakon
- SPECT/CT-Bildgebung
- 203Pb-RMX-VH-PIB
- RMX-VH-02
- lead-203
- radiolabeled peptide
- investigational radiopharmaceutical
- tumor-targeted radiopharmaceutical
- IDH-wildtype glioblastoma
- brain tumor targeting
- Astrocytoma grad IV
Zusätzliche relevante MeSH-Bedingungen
- Erkrankungen des endokrinen Systems
- Erkrankungen des Gehirns
- Erkrankungen des zentralen Nervensystems
- Erkrankungen des Nervensystems
- Neubildungen nach Standort
- Neubildungen
- Neubildungen nach histologischem Typ
- Neoplasmen des Verdauungssystems
- Erkrankungen des Verdauungssystems
- Neoplasmen der endokrinen Drüse
- Erkrankungen der Bauchspeicheldrüse
- Neubildungen, Drüsen und Epithelien
- Neubildungen, Neuroepithel
- Neuroektodermale Tumoren
- Neoplasmen, Keimzelle und Embryonal
- Neubildungen, Nervengewebe
- Neubildungen des Nervensystems
- Neubildungen des zentralen Nervensystems
- Neoplasmen der Bauchspeicheldrüse
- Glioblastom
- Gliom
- Neubildungen des Gehirns
- Astrozytom
- Diagnosetechniken und Verfahren
- Diagnose
- Tomographie
- Diagnostische Bildgebung
- Bildinterpretation, computergestützt
- Bildverbesserung
- Fotografie
- Tomographie, Emissionskomput
- Radionuklidbildgebung
- Diagnosetechniken, Radioisotop
- Tomographie, Emissions-Computertomographie, Einzelphotonen-
Andere Studien-ID-Nummern
- RMX-VH-02
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
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