- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT02556463
A Study of MEDI9197 in Subjects With Solid Tumors or CTCL and in Combination With Durvalumab and/or Palliative Radiation in Subjects With Solid Tumors
A Phase I, First-Time-in-Human Study of MEDI9197, a TLR 7/8 Agonist, Administered Intratumorally as a Single Agent in Subjects With Solid Tumors or CTCL and in Combination With Durvalumab and/or Palliative Radiation in Subjects With Solid Tumors
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Fase 1
Kontakter og lokationer
Studiesteder
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Ontario
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Toronto, Ontario, Canada, M5G 1Z6
- Research Site
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California
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San Francisco, California, Forenede Stater, 94115
- Research Site
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Colorado
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Aurora, Colorado, Forenede Stater, 80045
- Research Site
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Minnesota
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Minneapolis, Minnesota, Forenede Stater, 55455
- Research Site
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Missouri
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Saint Louis, Missouri, Forenede Stater, 63110
- Research Site
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New York
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New York, New York, Forenede Stater, 10029
- Research Site
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North Carolina
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Chapel Hill, North Carolina, Forenede Stater, 27599-7305
- Research Site
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Pennsylvania
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Philadelphia, Pennsylvania, Forenede Stater, 19104
- Research Site
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Texas
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Houston, Texas, Forenede Stater, 77030
- Research Site
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Villejuif, Frankrig, 94805
- Research Site
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria for All Subjects (Parts 1, 2 and 3)
- Written informed consent and any locally required authorizations.
- Male and female subjects at least 18 years at the time of screening.
- Adequate organ function within 14 days of enrollment confirmed by laboratory results.
- Systemic corticosteroids at doses exceeding 12 mg/day prednisone or equivalent.
- ECOG 0 or 1.
- Highly effective method of contraception from the date of the screening pregnancy test, and continued precautions for 6 months after the final dose of investigational product.
- Baseline Child-Pugh Score of A1 to B7.
- Life expectancy ≥ 12 weeks, as estimated by Royal Marsden Hospital Score of 0 or 1 at baseline.
Subjects with hepatocellular carcinoma (HCC) are eligible if the tumor is defined as nodular type 1 or 2 only.
Additional Inclusion Criteria for Subjects in Parts 1 and 3
- Metastatic/locally advanced solid tumor malignancy that has progressed on, is refractory to, or for which there is no standard of care therapy.
- For subjects with cutaneous/subcutaneous lesions, subjects must have more than one measurable target lesion, at baseline, with a minimum of one lesion that meets protocol specified criteria.
For subjects with deep-seated lesions, subjects must have more than one measurable target lesion at baseline (RECIST v1.1), with a minimum of one deep-seated lesion suitable for image-guided injection and that meets protocol specified criteria.
Additional Inclusion Criteria for Subjects in Part 2 (Closed to Enrollment as of Protocol Amendment 6)
- Clinical diagnosis of CTCL, including documentation of a skin biopsy with histological findings consistent with CTCL or unconfirmed diagnosis of CTCL with confirmation biopsy at screening.
- Stage IB, IIA, or IIB disease: T1, T2 or T3 (patches, plaques or tumors) with measurable lesions.
- Previous treatment with at least one standard therapy used to treat the stage of disease at study entry; Stage IB, IIA or IIB CTCL.
- Measurable skin disease with at least 2 lesions amenable to response assessment.
- At least one lesion must be amenable to injection, ie, ≥ 1.5 cm in the longest diameter.
Exclusion Criteria:
Any of the following would exclude the subject from participation in the study:
- Subjects who have received prior immunotherapy [(including but not limited to CTLA-4, oncolytic virus, oncolytic peptide-all require 100 day washout), programmed death ligand (PDL)-1, or programmed cell death 1 antagonists-both require 14 day washout)] are NOT permitted to enroll, with protocol exceptions.
- Pregnant or lactating.
- Active bacterial, fungal, or viral infections, including chronic or active hepatitis B, chronic or active hepatitis C, or active hepatitis A. Prior documented infections must have resolved.
- Active or prior documented autoimmune or inflammatory disorders, with exceptions per protocol. Includes known allergy to sesame oil and/or nuts.
- Immune-deficiency states - myelodysplastic disorders, marrow failures, human immunodeficiency virus (HIV) infection, history of solid organ transplant or bone marrow allograft, or recent pregnancy.
- Requires continuous (daily) anticoagulation or antiplatelet therapy (including anti aggregants), acetylsalicylic acid (ASA) or nonsteroidal anti-inflammatory drugs (NSAIDs).
- History of coagulopathy resulting in uncontrolled bleeding or other bleeding disorders.
- Rapidly progressing disease per protocol.
- Untreated or uncontrolled central nervous system (CNS) involvement.
- Any concurrent chemotherapy, immunotherapy, or biologic or hormonal therapy for cancer treatment; with exceptions per protocol.
- Unresolved toxicities from prior anticancer therapy, defined as having not resolved to NCI CTCAE v4.03 Grade 0 or 1, with exception of alopecia, vitiligo.
- Uncontrolled concurrent illness.
- Cardiac exclusions: New York Heart Association Class 3 or 4 congestive heart failure, uncontrolled hypertension, acute coronary syndrome within 6 months, clinical important cardiac arrhythmia, mean QTC interval corrected for heart rate >500ms.
- Major surgery within 4 weeks prior to study entry or still recovering from prior surgery.
- Receipt of live, attenuated vaccine within 28 days prior to study entry.
- Receipt of any systemic anticancer therapy not mentioned above within the last 2 weeks or 5 half-lives.
- Cognitive disorder such that informed consent cannot be obtained directly from the subject
- Subjects who have previously participated in this study and received MEDI9197, or concurrent enrollment in another clinical study involving an investigational treatment.
- Subjects who have received prior TLR agonists, both systemic and topical.
- Patients who have received prior therapeutic radiation within 28 days of dosing. All toxicities from prior radiotherapy must have resolved to ≤ Grade 1 or baseline prior to dosing.
- Body weight < 35 kg
- Subjects enrolling in Part 3 (ie, receiving durvalumab) must not have a history of interstitial lung disease or pneumonitis.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Ikke-randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
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Eksperimentel: Escalation MEDI9197
MEDI9197
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Subjects will receive MEDI9197 (every 4 weeks) as monotherapy (or MEDI9197 every 8 weeks + durvalumab every 4 weeks)(PA6)
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Eksperimentel: Escalation MEDI9197 with durvalumab
MEDI9197 in combination with durvalumab
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Subjects will receive MEDI9197 (every 4 weeks) as monotherapy (or MEDI9197 every 8 weeks + durvalumab every 4 weeks)(PA6)
Subjects will receive durvalumab every 4 weeks
Andre navne:
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Eksperimentel: Escalation MEDI9197 durvalumab radiation
MEDI9197 in combination with durvalumab and palliative radiation
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Subjects will receive MEDI9197 (every 4 weeks) as monotherapy (or MEDI9197 every 8 weeks + durvalumab every 4 weeks)(PA6)
Subjects will receive durvalumab every 4 weeks
Andre navne:
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Eksperimentel: MEDI9197 with palliative radiation
MEDI9197 in combination with palliative radiation
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Subjects will receive MEDI9197 (every 4 weeks) as monotherapy (or MEDI9197 every 8 weeks + durvalumab every 4 weeks)(PA6)
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
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Safety and tolerability as determined by assessment of dose limiting toxicities and the maximum tolerated dose or maximal assessed dose per protocol of MEDI9197 when administered by intratumoral injection to subjects with solid tumor cancers
Tidsramme: From time of informed consent through 4 weeks after last dose of investigational product
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The primary endpoint will be the number (%) of subjects with dose-limiting toxicities, adverse and serious adverse events and other safety parameters.
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From time of informed consent through 4 weeks after last dose of investigational product
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Safety and tolerability as determined by assessment of dose limiting toxicities and the maximum tolerated dose or maximal assessed dose per protocol of MEDI9197 when administered by intratumoral injection to subjects with CTCL
Tidsramme: From time of informed consent through 6 months after last dose of investigational product
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The primary endpoint will be the number (%) of subjects with dose-limiting toxicities, adverse and serious adverse events and other safety parameters.
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From time of informed consent through 6 months after last dose of investigational product
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Safety & tolerability as determined by dose limiting toxicities and maximum tolerated or assessed dose of MEDI9197 administered by IT injection in combo with durvalumab and durvalumab plus palliative radiation to subjects with solid tumor cancers.
Tidsramme: From time of informed consent through 90 days after last dose of investigational product
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The primary endpoint will be the number (%) of subjects with dose-limiting toxicities, adverse and serious adverse events and other safety parameters.
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From time of informed consent through 90 days after last dose of investigational product
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Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
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The maximum concentration of MEDI9197 after the first injection
Tidsramme: Pre-dose to 24 hours post first dose
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Pre-dose to 24 hours post first dose
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The apparent terminal half-life of MEDI9197
Tidsramme: Pre-dose to 24 hours post first dose
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Pre-dose to 24 hours post first dose
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Percent change from baseline in cluster of differentiation 8 tumor infiltrating lymphocytes in tumor tissue
Tidsramme: Baseline to Day 50
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Baseline to Day 50
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Percent change from baseline in serum inflammatory cytokine levels
Tidsramme: Pre-dose to end of study, up to 24 months
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Pre-dose to end of study, up to 24 months
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Percent change from baseline in tumor measurements
Tidsramme: Pre-dose to disease progression, up to 12 months
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Pre-dose to disease progression, up to 12 months
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Objective response rate
Tidsramme: Pre-dose to end of study, up to 24 months
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Pre-dose to end of study, up to 24 months
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Duration of response
Tidsramme: Pre-dose to end of study, up to 24 months
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Pre-dose to end of study, up to 24 months
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Percent change from baseline in CAILDS for subjects with CTCL
Tidsramme: Pre-dose to disease progression, up to 12 months
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Pre-dose to disease progression, up to 12 months
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Percent change from baseline in mSWAT scored for subjects with CTCL
Tidsramme: Pre-dose to disease progression, up to 12 months
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Pre-dose to disease progression, up to 12 months
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Percent change from baseline in Investigator Global Assessment (IGA) for subjects with CTCL
Tidsramme: Pre-dose to disease progression, up to 12 months
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Pre-dose to disease progression, up to 12 months
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Percent change from baseline in Subject Global Assessment (SGA) for subjects with CTCL
Tidsramme: Pre-dose to disease progression, up to 12 months
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Pre-dose to disease progression, up to 12 months
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Samarbejdspartnere og efterforskere
Sponsor
Publikationer og nyttige links
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- D6410C00001
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Kliniske forsøg med MEDI9197
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National Institute of Allergy and Infectious Diseases...Duke University; National Institutes of Health (NIH); Department of Health... og andre samarbejdspartnereTrukket tilbage