- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT07859592
Labyrinthin Vaccination in Veterans With Lung Adenocarcinoma
Labyrinthin Vaccination for Patients With Lung Adenocarcinomas
This phase 2 trial tests the safety and effectiveness of a cancer vaccine called LabVax 3(22)-23 and GM-CSF in combination with pembrolizumab in treating adenocarcinoma that has spread to other places in the body (advanced stage). LabVax 3(22)-23 is designed to target a specific antigen (labyrinthin), which is a protein found on the surface of adenocarcinoma tumor cells. Labyrinthin is a protein that is not expressed on normal cells in the skin, lungs, salivary glands, pancreas, nor other tissues. In adenocarcinoma, the tumor cells produce too much labyrinthin causing them to express this protein on the surface of the tumor cells. One way to control the growth of these tumor cells is to teach the immune system to generate an immune response against the labyrinthin protein by vaccination against labyrinthin. GM-CSF, or sargramostim, is a protein that acts as a white blood cell growth factor. It has also been shown to stimulate immune system. Thus, administration of GM-CSF may help to boost the immune system response when given together with the vaccine. This study may improve the general knowledge about LabVax 3(22)-23 and how the body may generate an immune response to kill adenocarcinoma tumor cells. In the second phase of the study, participants will also receive pembrolizumab, which may improve anti-cancer activity when given with LabVax 3(22)-23 and GM-CSF.
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
Phase 2: Up to 30 participants with advanced/ metastatic or recurrent lung adenocarcinoma. Pembrolizumab will be given intravenously every 3 weeks for up to 12 cycles on Day 1 of Weeks 1, 4, 7, 10, 13, 16, 19, 22, 25, 28, 31, and 34. Subjects will be given LabVax 3(22)-23 (intradermally) and adjuvant GM-CSF (subcutaneously) on weeks 7, 8, 10, 13, and 19. Participants will receive study treatment over 34 weeks if tolerating the treatment without tumor progression; a safety follow-up visit will occur 30 days post-last dose of study treatment. The participant's chart will be reviewed for up to 12 months post-last dose of study treatment. The study will be terminated if safety is insufficient or if response is insufficient in the first expansion.
Tipo di studio
Iscrizione (Stimato)
Fase
- Fase 2
Contatti e Sedi
Contatto studio
- Nome: Tianhong Li, MD
- Numero di telefono: (707) 437-1802
- Email: tianhong.Li@va.gov
Backup dei contatti dello studio
- Nome: Manuel Alcazar, RN
- Numero di telefono: (916) 843-2776
- Email: manuel.alcazar@va.gov
Luoghi di studio
-
-
California
-
Long Beach, California, Stati Uniti, 90822
- VA Long Beach Healthcare System, Long Beach, CA
-
Contatto:
- Pankaj Gupta
- Numero di telefono: 12243 562-826-8000
- Email: Pankaj.Gupta@va.gov
-
Sacramento, California, Stati Uniti, 95655-4200
- VA Northern California Health Care System, Mather, CA
-
Contatto:
- Jefferson Lee
- Numero di telefono: (916) 843-2769
- Email: Jefferson.Lee2@va.gov
-
Contatto:
- Jerry L Nadler, MD
- Numero di telefono: (916) 843-2776
- Email: Jerry.Nadler@va.gov
-
Investigatore principale:
- Tianhong Li, MD
-
San Francisco, California, Stati Uniti, 94121-1563
- San Francisco VA Medical Center, San Francisco, CA
-
Contatto:
- Sunny Wang
- Numero di telefono: 23380 415-221-4810
- Email: Sunny.wang@va.gov
-
-
Missouri
-
Kansas City, Missouri, Stati Uniti, 64128-2226
- Kansas City VA Medical Center, Kansas City, MO
-
Contatto:
- Chao Huang
- Numero di telefono: 650-493-5000
- Email: Chao.Huang@va.gov
-
-
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria:
- Ability to understand and willingness to sign an informed consent form
- Histologically confirmed diagnosis of lung adenocarcinoma
- Subjects with advanced/metastatic or recurrent solid tumors, with measurable or non-measurable disease as determined by Response Evaluation Criteria In Solid Tumors (RECIST) version 1.1 are eligible for participation.
- Histologically confirmed diagnosis of labyrinthin-positive lung adenocarcinoma
- Received at least one line of anti-PD-1 or anti-PD-L1 therapy for any stage of non-Small Cell Lung Cancer (NSCLC). Anti-PD-1 or anti-PD-L1 may have been given alone or in combination with other therapy
- Progressed on at least one line of therapy if participant has a known sensitizing mutation for which an FDA-approved targeted therapy for NSCLC exists (e.g., EGFR, ALK, ROS1, BRAF, RET, NTRK, and MET sensitizing mutations)
- All subjects must be candidates for pembrolizumab therapy
- Subjects can either have progressed, had no response, or intolerance to prior cancer therapy. Patients must have recovered from all clinically significant treatment-related toxicities to grade 1 or less, except chemotherapy-associated peripheral neuropathy (motor or sensory), or endocrine-related AE, in which recovery to ≤ Grade 2 is allowed. For endocrine-related AEs, physiological doses of replacement therapy (e.g., levothyroxine, insulin, hydrocortisone, or other replacement therapy for adrenal or pituitary insufficiency, etc.) are allowed.
- No limit on prior lines of therapy for metastatic disease. Prior chemotherapy, immunotherapy (including pembrolizumab) or molecularly targeted therapy must have been completed at least 3 weeks prior to initiating study treatment. Prior palliative radiation must have been completed at least 2 weeks prior to initiating study treatment.
- Subjects with known untreated, active brain and/or leptomeningeal metastases are excluded. Subjects with treated brain metastasis who are neurologically stable and off steroids for at least one week are eligible.
- Eastern Cooperative Oncology Group (ECOG) performance status of 0-1
- Life expectancy of ≥ 6 months at the time of initiating study treatment
- Subjects must demonstrate adequate organ function as defined below:
- Absolute neutrophil count (ANC) greater than or equal to 1,000 cells /Liter (L)
- Absolute lymphocyte counts (ALCs) greater than or equal to 600 cells per microliter
- Platelets greater than or equal to 75,000 cells/L
- Creatinine clearance as calculated per Cockcroft-Gault or Modification of Diet in Renal Disease (MDRD) formula ≥30 milliliters(mL)/minute (min)
- Total bilirubin ≤ 1.5 times the upper limit of normal (ULN), OR direct bilirubin ≤ ULN for participants with total bilirubin levels >1.5 times the ULN
- Aspartate aminotransferase or serum glutamic-oxaloacetic transaminase (AST or SGOT) and alanine aminotransferase or serum glutamic-pyruvic transaminase (ALT or SGPT) ≤2.5 times the ULN, OR ≤5 times the ULN for participants with liver metastases
- Because the effects of the study treatment on the unborn fetus or nursing infant are unknown, pregnant and nursing women are ineligible. Women of childbearing age must have a negative urine or serum pregnancy test-Human Chorionic Gonadotropin(HCG) within 72 hours prior to receiving the first dose of study medication. If the urine test is positive or cannot be confirmed as negative, a serum pregnancy test will be required.
- Confirmation of adequate archival tumor specimens (i.e., sufficient specimens for ten, 5-7 micrometer (µm) thick, unstained sections)
Exclusion Criteria:
- Subjects who have autoimmune diseases that require immunosuppressive medications other than prednisone ≤ 10 milligram (mg) daily or equivalent. Physiological doses of replacement therapy (e.g., levothyroxine, insulin, hydrocortisone, or other replacement therapy for adrenal or pituitary insufficiency, etc.) are not considered a form of immunosuppressant and are allowed.
- Prior splenectomy
- Pregnant or nursing women
- Any medical condition including additional malignancies, laboratory abnormalities, or psychiatric illness that in the opinion of the investigator would prevent the subject from participating and adhering to study related procedures.
- Uncontrolled concomitant disease that in the opinion of the investigator would interfere with the subject's safety or compliance on trial
- Severe infection that in the opinion of the investigator would interfere with subject safety or compliance on trial within 4 weeks prior to enrollment
- Subjects who have contraindications to GM-CSF injections according to the package insert (e.g., subjects with excessive leukemic myeloid blasts in the bone marrow or peripheral blood (≥ 10%); known hypersensitivity to GM-CSF, yeast-derived products or any component of the product)
Additional exclusion criteria for participants entering Phase 2:
- Is receiving systemic steroid therapy (> 10 mg prednisone oral daily or equivalent) or any other form of immunosuppressive therapy within 7 days prior to the first dose of trial treatment
- Has a known history of active TB (Bacillus Tuberculosis)
- Hypersensitivity to pembrolizumab or any of its excipients
- Has had a prior anti-cancer monoclonal antibody (mAb) within 3 weeks prior to study Day 1 or who has not recovered (i.e., ≤ Grade 1 or at baseline) from adverse events due to agents administered more than 3 weeks earlier
- Has had prior chemotherapy, targeted therapy, or radiation therapy within 2 weeks prior to study Day 1 or who has not recovered (i.e., ≤ Grade 1 or at baseline) from adverse events due to a previously administered agent
Note: Subjects with ≤ Grade 2 neuropathy are an exception to this criterion and may qualify for the study.
Note: If subjects received major surgery, they must have recovered adequately from the toxicity and/or complications from the intervention prior to starting therapy.
- Has known untreated, symptomatic central nervous system (CNS) metastases and/or carcinomatous meningitis. Subjects with previously treated brain metastases may participate provided they are stable (without evidence of progression by imaging for at least four weeks prior to the first dose of trial treatment and any neurologic symptoms have returned to baseline), have no evidence of new or enlarging brain metastases requiring treatment, and are not using steroids (> 10 mg prednisone oral daily or equivalent) for at least 7 days prior to trial treatment. This exception does not include carcinomatous meningitis which is excluded regardless of clinical stability.
- Has known history of ≥ grade 3 pneumonitis or interstitial lung disease related to radiation, immunotherapy, chemotherapy, or targeted therapy
- Has an active infection requiring systemic therapy
- Has a history or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the trial, interfere with the subject's participation for the full duration of the trial, or is not in the best interest of the subject to participate, in the opinion of the treating investigator
- Has known active Hepatitis B (e.g., Hepatitis B Surface Antigen (HBsAg) reactive) or Hepatitis C (e.g., HCV RNA [qualitative] is detected)
- Has received a live vaccine within 30 days of planned start of study therapy
Note: Seasonal influenza vaccines for injection are generally inactivated flu vaccines and are allowed; however intranasal influenza vaccines (e.g., Flu-Mist®) are live attenuated vaccines, and are not allowed. Corona Virus Disease (COVID) vaccines are allowed.
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: N / A
- Modello interventistico: Assegnazione sequenziale
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Sperimentale: LabVax 3(22)-23 and GM-CSF (immunoadjuvant) in combination with pembrolizumab
LabVax 3(22)-23, and GM-CSF (adjuvant) in combination with pembrolizumab in subjects with advanced/metastatic or recurrent advanced/metastatic or recurrent lung adenocarcinoma. |
LabVax 3(22)-23, and GM-CSF (adjuvant) in combination with pembrolizumab in subjects with advanced/metastatic or recurrent advanced/metastatic or recurrent lung adenocarcinoma. |
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Objective Response Rate (ORR) as Assessed According to Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST v 1.1)
Lasso di tempo: 7 years
|
To assess antitumor activity per RECIST 1.1 of LabVax 3(22)-23 administered at the Recommended Phase 2 Dose (RP2D) and adjuvant GM-CSF in combination with pembrolizumab in participants with advanced/metastatic or recurrent lung adenocarcinoma who have received at least one line of immune checkpoint inhibitor therapy. |
7 years
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Dose-limiting toxicity (DLTs)
Lasso di tempo: 7 years
|
Number of participants with dose-limiting toxicities (DLTs) during the safety lead-in period |
7 years
|
|
Adverse events
Lasso di tempo: 7 years
|
Number of participants with treatment-emergent adverse events assessed according to CTCAE v6.0 |
7 years
|
|
Median PFS
Lasso di tempo: 7 years
|
Median progression-free survival (PFS) in months |
7 years
|
|
6-month PFS
Lasso di tempo: 7 years
|
Progression-free survival rate at 6 months in percentage of participants |
7 years
|
|
12-month PFS
Lasso di tempo: 7 years
|
Progression-free survival rate at 12 months in percentage of participants |
7 years
|
|
Median OS
Lasso di tempo: 7 years
|
Median overall survival (OS) in months |
7 years
|
Altre misure di risultato
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Labyrinthin immunohistochemistry (IHC) expression
Lasso di tempo: 7 years
|
To measure the expression of Labyrinthin by IHC and the effects of LabVax 3(22)-23 in combination with pembrolizumab |
7 years
|
Collaboratori e investigatori
Collaboratori
Investigatori
- Investigatore principale: Tianhong Li, MD, VA Northern California Health Care System, Mather, CA
Pubblicazioni e link utili
Collegamenti utili
Studiare le date dei record
Studia le date principali
Inizio studio (Stimato)
Completamento primario (Stimato)
Completamento dello studio (Stimato)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
- Processi patologici
- Vaccini contro il cancro
- Carcinoma
- Neoplasie
- Adenocarcinoma
- Vaccini
- Citochine
- pembrolizumab
- Peptidi
- Carboidrati
- Neoplasie, ghiandolari ed epiteliali
- Neoplasie per tipo istologico
- Proteine
- Metastasi neoplastica
- Fattori biologici
- Glicoproteina
- Processi neoplastici
- sargramostim
- Fattori di crescita delle cellule ematopoietiche
- Condizioni patologiche, segni e sintomi
- Prodotti biologici
- Amino Acids, Peptides, and Proteins
- Complex Mixtures
- Glycoconjugates
- Intercellular Signaling Peptides and Proteins
- Colony-Stimulating Factors
Termini MeSH pertinenti aggiuntivi
- Neoplasie
- Carcinoma
- Metastasi neoplastica
- Adenocarcinoma
- Neoplasie per tipo istologico
- Neoplasie, ghiandolari ed epiteliali
- Processi patologici
- Processi neoplastici
- Condizioni patologiche, segni e sintomi
- Distrofia muscolare dei cingoli, tipo 2C
- Peptidi
- Aminoacidi, peptidi e proteine
- Proteine
- Preparati farmaceutici
- Azioni e usi chimici
- Fattori biologici
- Carboidrati
- Usi speciali di sostanze chimiche
- Aiuti farmaceutici
- Peptidi e proteine di segnalazione intercellulare
- Glicoproteine
- Glicoconiugati
- Fattori stimolanti le colonie
- Fattori di crescita delle cellule ematopoietiche
- Citochine
- Adiuvanti, farmaceutico
- pembrolizumab
- Fattore stimolante le colonie di granulociti-macrofagi
Altri numeri di identificazione dello studio
- ONCB-006-26S
- I01RD001080-01A1 (Altro numero di sovvenzione/finanziamento: eRA)
Piano per i dati dei singoli partecipanti (IPD)
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Informazioni su farmaci e dispositivi, documenti di studio
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Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .