Étude de phase I/IIa pour AZD5335 en monothérapie et en association avec des agents anticancéreux chez des participants atteints de tumeurs solides (FONTANA)
FONTANA : Une étude modulaire de phase I/IIa, ouverte et multicentrique pour évaluer l'innocuité, la tolérabilité, la pharmacocinétique et l'efficacité préliminaire de doses croissantes d'AZD5335 en monothérapie et en association avec des agents anticancéreux chez des participants atteints de tumeurs solides
This research is designed to determine if experimental treatment with Antibody-drug conjugate, AZD5335, alone, or in combination with anti-cancer agents is safe, tolerable, and has anti-cancer activity in patients with advanced tumors
Aperçu de l'étude
Statut
Les conditions
Description détaillée
This study is a Phase I/IIa modular, open-label, multi-center study of AZD5335 administered either as monotherapy or in combination with other anti-cancer agents in participants with advanced solid malignancies
Type d'étude
Inscription (Estimé)
Phase
- Phase 2
- La phase 1
Contacts et emplacements
Coordonnées de l'étude
- Nom: AstraZeneca Clinical Study Information Center
- Numéro de téléphone: 1-877-240-9479
- E-mail: information.center@astrazeneca.com
Lieux d'étude
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Berlin, Allemagne, 13353
- Recrutement
- Research Site
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Essen, Allemagne, 45136
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- Research Site
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Freiburg im Breisgau, Allemagne, 79106
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Hanover, Allemagne, 30625
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Leipzig, Allemagne, 04103
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Mannheim, Allemagne, 68167
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Regensburg, Allemagne, 93053
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Liverpool, Australie, 2170
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Melbourne, Australie, 3000
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Alberta
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Edmonton, Alberta, Canada, T6G 1Z2
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Ontario
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London, Ontario, Canada, N6A 5W9
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Toronto, Ontario, Canada, M5G 2M9
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Quebec
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Montreal, Quebec, Canada, H4A 3J1
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Montreal, Quebec, Canada, H2X 0A9
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Chengdu, Chine, 610041
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Chongqing, Chine, 400030
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Guangzhou, Chine, 510060
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Guangzhou, Chine, 510000
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Jinan, Chine, 250117
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Xi'an, Chine, 710061
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Zhengzhou, Chine, 450008
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Seoul, Corée du Sud, 03080
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Seoul, Corée du Sud, 06351
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Barcelona, Espagne, 8035
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Madrid, Espagne, 28041
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Madrid, Espagne, 28050
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Málaga, Espagne, 29010
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Haifa, Israël, 3109601
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Ramat Gan, Israël, 52621
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Hidaka-shi, Japon, 350-1298
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Kashiwa, Japon, 227-8577
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Kōtoku, Japon, 135-8550
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Sunto-gun, Japon, 411-8777
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Tokyo, Japon, 104-0045
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Cambridge, Royaume-Uni, CB2 0XY
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Glasgow, Scotland, Royaume-Uni, G12 0YN
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London, Royaume-Uni, SE1 9RT
- Pas encore de recrutement
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London, Royaume-Uni, SW3 6JJ
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Sutton, Royaume-Uni, SM2 5PT
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Taichung, Taïwan, 40705
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Tainan, Taïwan, 70403
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Taipei, Taïwan, 10002
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Taipei, Taïwan, 11259
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Ankara, Turquie (Türkiye), 06800
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Ankara, Turquie (Türkiye), 06050
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Ankara, Turquie (Türkiye), 06200
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Istanbul, Turquie (Türkiye), 34718
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California
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Duarte, California, États-Unis, 91010
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Irvine, California, États-Unis, 92618
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La Jolla, California, États-Unis, 92093
- Retiré
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Colorado
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Aurora, Colorado, États-Unis, 80045
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Kentucky
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Louisville, Kentucky, États-Unis, 40202
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Massachusetts
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Boston, Massachusetts, États-Unis, 02114
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Michigan
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Detroit, Michigan, États-Unis, 48201
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Ohio
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Columbus, Ohio, États-Unis, 43201
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Oregon
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Portland, Oregon, États-Unis, 97239
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Rhode Island
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Providence, Rhode Island, États-Unis, 02903
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Providence, Rhode Island, États-Unis, 02905
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Texas
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Houston, Texas, États-Unis, 77030
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Virginia
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Fairfax, Virginia, États-Unis, 22031
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Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
Core Inclusion Criteria:
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Capable of giving signed informed consent, which includes compliance with the requirements and restrictions listed in the ICF and in this protocol.
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Provision of signed and dated written Optional Genetic Research Information informed consent prior to collection of samples for optional genetic research that supports Genomic Initiative. Participants who do not provide informed consent for Optional Genetic Research may still be enrolled in the study.
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Participant must be ≥ 18 years at the time of signing the informed consent.
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Willing to provide adequate archival and/or baseline tumor sample as applicable per module-specific criteria.
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For participants who have previously received targeted therapies such as ADCs, a fresh baseline biopsy will be required unless the most recent archival tissue sample was collected after receipt of such treatment.
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Eastern Cooperative Oncology Group Performance Status of 0 or 1.
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Participants with advanced solid tumors must have received prior adequate therapy in accordance with local practice for their tumor type and stage of disease, or, in the opinion of the Investigator, a clinical trial is the best option for the next treatment based on response and/or tolerability to prior therapy. Participants with contraindications or who refuse therapy in accordance with local practice may also be considered provided that it is documented that he/she was informed about all therapeutic options.
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Participants must have measurable disease per RECIST v1.1,
- A previously irradiated lesion can be considered a target lesion if the lesion is progressing and well defined.
- For participants who undergo biopsies at screening and/or on treatment, it is preferred though not required, that the biopsied lesion, be distinct from any target lesion used in the RECIST v1.1 evaluation.
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Life expectancy ≥ 12 weeks.
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Adequate organ and marrow function.
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Contraceptive use by men or women should be consistent with local regulations regarding the methods of contraception for those participating in clinical studies.
(a) Male participants: (i) Male participants who are sexually active with a female partner of childbearing potential must use a male condom (plus an additional contraceptive method) post-screening for at least 8 months following the last dose of study intervention. It is strongly recommended for the female partner of a male participant to also use a highly effective method of contraception throughout this period. In addition, male participants must refrain from freezing or donating sperm while on study and for 8 months following the last dose of study intervention.
(b) Female participants : (i) Females of childbearing potential must have a negative serum pregnancy test result within 72 hours prior to receiving the first dose of study intervention and a negative urine or serum pregnancy test prior to starting their next cycle of treatment. If the urine test is positive or cannot be confirmed as negative, a serum pregnancy test will be required.
(ii) (ii) Sex and Contraceptive/Barrier Requirements: Highly effective birth control methods include: Total sexual abstinence is an acceptable method provided it is the usual lifestyle of the participant (defined as refraining from heterosexual intercourse during the entire period of risk associated with the study treatments) [(periodic abstinence e.g., calendar, ovulation, symptothermal, post-ovulation methods), declaration of abstinence for the duration of exposure to study intervention, and withdrawal are not acceptable methods of contraception], a vasectomized partner, Implanon®, bilateral tubal occlusion, intrauterine device/levonorgestrel intrauterine system, Depo Provera™ injections, oral contraceptive associated with inhibition of ovulation, and Evra Patch™, Xulane™, or NuvaRing®.
Female participants of childbearing potential who are sexually active with a non-sterilized male partner must agree to use one highly effective method of birth control (defined as one that can achieve a failure rate of less than 1% per year when used consistently and correctly), from enrolment throughout the study and for 8 months following the last dose of study intervention. The male partner of a female participant of childbearing potential must also use a male condom (plus spermicide, if available) throughout this period. Cessation of contraception after this point should be discussed with a responsible physician. In addition, female participants must not donate or retrieve for their own use, ova while on study and for 8 months following the last dose of study intervention.
Core Exclusion Criteria:
- Patients with spinal cord compression or a history of leptomeningeal carcinomatosis.
- Patients with brain metastases unless, asymptomatic, stable, and not requiring continuous corticosteroids at a dose of > 10 mg prednisone/day or equivalent for at least 4 weeks prior to first dose of study intervention.
- Treatment with any of the protocol defined medications, without adequate washout periods or time before the first dose of study intervention.
- Unresolved toxicities of Grade ≥ 2 (National Cancer Institute [NCI] CTCAE v5.0) from prior therapy (excluding vitiligo, alopecia, and endocrine disorders that are controlled with replacement hormone therapy). Participants with stable ≤ Grade 2 neuropathy are eligible.
- Active infection, including tuberculosis and infections with hepatitis B virus (HBV; verified by known positive hepatitis B surface antigen [HBsAg] result), hepatitis C virus (HCV) or known HIV infection that is not well controlled. All of the following criteria are required to define an HIV infection that is well controlled: undetectable viral RNA, CD4+ count ≥ 350/mm3, no history of acquired immune deficiency syndrome-defining opportunistic infection within the past 12 months, and stable for at least 4 weeks on the same anti-HIV medications (meaning there are no expected further changes in that time to the number or type of antiretroviral drugs in the regimen).
Patients with a past or resolved HBV/HCV infection are eligible if:
- Negative for HBsAg and positive for anti-hepatitis B virus core protein (HBc) or
- Are HBsAg + with chronic HBV infection (lasting 6 months or longer) and meet conditions i-iii below:
(i) HBV DNA viral load <100 IU/mL. (ii) Have normal transaminase values, or, if liver metastases are present, abnormal transaminases, with a result of aspartate aminotransferase (AST)/alanine aminotransferase (ALT) <3 x upper limit of normal (ULN), which are not attributable to HBV infection.
(iii) Start or maintain antiviral treatment if clinically indicated as per the Investigator or as per local guideline.
Note for Japan: Japanese patients with positive anti-HBs/anti-HBc and negative HBsAg will be assessed following local guidelines.
(c) Participants testing positive for HCV antibody are eligible only if the polymerase chain reaction test result is negative for HCV RNA.
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Patient has active ILD/pneumonitis or has a history of (non-infectious) ILD/pneumonitis that required oral or IV steroids or supplemental oxygen, or where suspected ILD/pneumonitis cannot be ruled out by imaging at screening.
- Patients with a history of radiation pneumonitis which has clinically and radiologically resolved and not requiring treatment with steroids may be eligible.
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History of another malignancy except for:
- Malignancy treated with curative intent and with no known active disease for at least 2 years prior to screening of study intervention and with low potential risk for recurrence.
- Adequately treated non-melanoma skin cancer or lentigo maligna without evidence of disease.
- Adequately treated carcinoma in situ without evidence of disease.
- Localized non-invasive solid organ primary disease under surveillance.
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Patients with any of the following cardiac criteria:
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History of arrhythmia (such as multifocal premature ventricular contractions, bigeminy, trigeminy, and ventricular tachycardia), which is symptomatic or requires treatment NCI CTCAE v5.0 Grade 3 except for:
(i) Rate controlled asymptomatic atrial fibrillation.
- NOTE: significant abnormalities in serum electrolytes that can increase the risk of arrhythmic events (ie, sodium, potassium, calcium, and magnesium) should be corrected before starting the study intervention.
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Uncontrolled hypertension.
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Acute coronary syndrome/acute myocardial infarction, unstable angina pectoris, coronary intervention procedure with percutaneous coronary intervention, or coronary artery bypass grafting within 6 months of screening.
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History of brain perfusion problems (eg, carotid stenosis) or stroke, or transient ischemic attack in the last 6 months prior to screening.
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Symptomatic heart failure (as defined by New York Heart Association class ≥ 2).
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Prior or current diagnosis of cardiomyopathy considered clinically relevant per investigator's judgement.
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Severe uncorrected valvular heart disease.
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Mean resting QTcF > 470 msec obtained from triplicate electrocardiograms (ECGs) and averaged, recorded within 5 minutes.
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Any factor that, in the opinion of the investigator, increases the proarrhythmic risk of QT prolongation, such as congenital long QT syndrome, family history of long QT syndrome, hypertrophic cardiomyopathy, or unexplained sudden cardiac death under 40 years of age.
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Uncontrolled and/or unresolved intercurrent illness within 12 months prior to screening, including but not limited to serious chronic gastrointestinal conditions associated with diarrhea, or illness (including psychiatric illness) and/or social situations, in the opinion of the investigator, that would limit compliance with study requirements and activities, substantially increase risk of incurring AEs or compromise the ability of the participant to give written informed consent.
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Substance abuse or any other medical conditions that would increase the safety risk to the participant or interfere with participation of the participant or evaluation of the clinical study in the opinion of the Investigator.
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Receipt of live attenuated vaccine within 30 days prior to the first dose of study intervention. Note: Participants, if enrolled, should not receive live vaccine whilst receiving study intervention and up to 3 months after the last dose of study intervention. Participants can receive Coronavirus (COVID)-19 vaccines, at the discretion of the Investigator, following a benefit/risk evaluation for the individual participant and in accordance with local rules and regulations and vaccination guidelines. Note: If a COVID-19 vaccine is administered it should be done > 72 hours prior to study intervention initiation or after completion of the DLT period.
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For women only - currently pregnant (confirmed with positive pregnancy test or suspected), lactating, breastfeeding, or intention to become pregnant during the study period.
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Concurrent enrolment in another clinical study, unless it is an observational (non interventional) clinical study or during the follow-up period of an interventional study. Exception: Diagnostic imaging evaluation studies (e.g. PET) may be allowed subject to case-by-case discussion with the Sponsor.
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Patients with a known hypersensitivity to study intervention or any of the excipients of the product.
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Involvement in the planning and/or conduct of the study (applies to both AstraZeneca staff and/or staff at the study site).
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Judgment by the Investigator that the patient should not participate in the study if the patient is unlikely to comply with study procedures, restrictions and requirements.
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Previous enrolment in the present study. **Other module specific criteria may apply
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation séquentielle
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
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Expérimental: Module 1: Torvu-sam Monotherapy
Torvu-sam Monotherapy |
IV Antibody-drug conjugate
Autres noms:
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Expérimental: Module 2: Torvu-sam + Saruparib
Torvu-sam + Saruparib |
IV Antibody-drug conjugate
Autres noms:
Oral PARP inhibitor
Autres noms:
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Expérimental: Module 3: Torvu-sam + Bevacizumab
Torvu-sam + Bevacizumab |
IV Antibody-drug conjugate
Autres noms:
IV Monoclonal antibody
Autres noms:
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Expérimental: Module 4: Torvu-sam + Carboplatin +/- Bevacizumab
Torvu-sam + Carboplatin +/- Bevacizumab |
IV Antibody-drug conjugate
Autres noms:
IV Monoclonal antibody
Autres noms:
IV Alkylating agent
Autres noms:
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Expérimental: Module 5: Torvu-sam + Palacaparib +/- Bevacizumab
Torvu-sam + Palacaparib +/- Bevacizumab |
IV Antibody-drug conjugate
Autres noms:
IV Monoclonal antibody
Autres noms:
Oral PARP inhibitor
Autres noms:
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Expérimental: Module 6: Torvu-sam + Pembrolizumab +/- Palacaparib
Torvu-sam + Pembrolizumab +/- Palacaparib |
IV Antibody-drug conjugate
Autres noms:
Oral PARP inhibitor
Autres noms:
IV Biologic |
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Number of participants with adverse events/serious adverse events
Délai: From time of Informed Consent to 30 days post last dose.
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Number of participants with incidence of adverse events and with serious adverse events including changes from baseline in laboratory parameters, vital signs, ECGs, and physical examination. |
From time of Informed Consent to 30 days post last dose.
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The number of participants with dose limiting toxicity(DLT), as defined in the protocol
Délai: From the first dose of torvu-sam on Cycle 1 Day 1 up to and including the planned end of Cycle 1 (At the end of 21 days)
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A DLT is defined as any ≥ Grade 3 treatment-emergent AE that occurs during the DLT evaluation period, not attributable to the underlying disease or extraneous causes (as defined in the protocol) |
From the first dose of torvu-sam on Cycle 1 Day 1 up to and including the planned end of Cycle 1 (At the end of 21 days)
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Objective Response Rate (ORR)
Délai: From time of Informed Consent to progressive disease or withdrawal of consent.(approx 2 years)
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The percentage of participants with a confirmed CR or PR according to RECIST v1.1 criteria. |
From time of Informed Consent to progressive disease or withdrawal of consent.(approx 2 years)
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Duration of Response (DoR)
Délai: From the first documented response to confirmed progression or death in the absence of disease progression.(approx 2 years)
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The time from the date of first response until date of disease progression or death in the absence of disease progression. |
From the first documented response to confirmed progression or death in the absence of disease progression.(approx 2 years)
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Disease Control Rate (DCR)
Délai: From time of Informed Consent until progression.(approx 15 weeks)
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The percentage of participants who have a best objective response of confirmed CR or PR or who have SD for at least 15 weeks after start of treatment (to allow for an early assessment within the assessment window). |
From time of Informed Consent until progression.(approx 15 weeks)
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Progression free Survival (PFS)
Délai: From time of first dose of torvu-sam or anti-cancer study agent until the date of objective disease progression or death (by any cause in the absence of progression) (approx 2 years)
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Progression-free survival is defined as the time from the start of treatment until the date of objective disease progression or death (by any cause in the absence of progression), regardless of whether the participant withdraws from assigned therapy or receives another anti-cancer therapy prior to progression. Participants who have not progressed or died at the time of analysis will be censored at the time of the latest date of assessment from their last evaluable RECIST v1.1 assessment |
From time of first dose of torvu-sam or anti-cancer study agent until the date of objective disease progression or death (by any cause in the absence of progression) (approx 2 years)
|
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Overall Survival (OS)
Délai: From time of first dose of torvu-sam or anti-cancer study agent until death due to any cause (approx 2 years)
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The time until death due to any cause. |
From time of first dose of torvu-sam or anti-cancer study agent until death due to any cause (approx 2 years)
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Module 1: Pharmacokinetics of torvu-sam
Délai: From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam (approx 12 weeks) through 30-day follow-up
|
The plasma concentrations of torvu-sam, total antibody, and total unconjugated payload. |
From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam (approx 12 weeks) through 30-day follow-up
|
|
Module 1: Pharmacokinetics of torvu-sam: Area Under the concentration-time curve(AUC)
Délai: From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam (approximately 12 weeks) through 30-day follow-up
|
Area under the plasma concentration-time curve |
From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam (approximately 12 weeks) through 30-day follow-up
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Module 1: Pharmacokinetics of torvu-sam: Maximum plasma concentration of the study drug (Cmax)
Délai: From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam (approximately 12 weeks) through 30-day follow-up
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Maximum observed plasma concentration of the study drug |
From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam (approximately 12 weeks) through 30-day follow-up
|
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Module 1: Pharmacokinetics of torvu-sam: Time to maximum plasma concentration of the study drug (T-max)
Délai: From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam (approximately 12 weeks) through 30-day follow-up
|
Time to maximum observed plasma concentration of the study drug |
From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam (approximately 12 weeks) through 30-day follow-up
|
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Module 1: Pharmacokinetics of torvu-sam: Clearance
Délai: From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam (approximately 12 weeks) through 30-day follow-up
|
A pharmacokinetic measurement of the volume of plasma from which the study drug is completely removed per unit time. |
From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam (approximately 12 weeks) through 30-day follow-up
|
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Module 1: Pharmacokinetics of torvu-sam: Terminal elimination half-life (t 1/2)
Délai: From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam (approximately 12 weeks) through 30-day follow-up
|
Terminal elimination half-life. |
From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam (approximately 12 weeks) through 30-day follow-up
|
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Module 1: To investigate baseline and on treatment changes in target expression.
Délai: Baseline and predicted intervals throughout the administration of torvu-sam (approx 2 years)
|
The clinical activity by baseline and on-treatment changes in tumor target expression. |
Baseline and predicted intervals throughout the administration of torvu-sam (approx 2 years)
|
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Module 2: Pharmacokinetics of torvu-sam and saruparib when given in combination.
Délai: From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam and saruparib (approx 12 weeks) through 30-day follow-up
|
The plasma concentrations of torvu-sam, total antibody, and total unconjugated payload. |
From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam and saruparib (approx 12 weeks) through 30-day follow-up
|
|
Module 3: Pharmacokinetics of torvu-sam and bevaczizumab when given in combination.
Délai: From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam and bevacizumab (approx 12 weeks) through 30-day follow-up
|
The plasma concentrations of torvu-sam, total antibody, and total unconjugated payload. |
From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam and bevacizumab (approx 12 weeks) through 30-day follow-up
|
|
Module 4: Pharmacokinetics of torvu-sam and carboplatin (+/- bevacizumab) when given in combination.
Délai: From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam and carboplatin (+/- bevacizumab) (approx 12 weeks) through 30-day follow-up
|
The plasma concentrations of torvu-sam, total antibody, and total unconjugated payload. |
From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam and carboplatin (+/- bevacizumab) (approx 12 weeks) through 30-day follow-up
|
|
Module 5: Pharmacokinetics of torvu-sam and palacaparib (+/- bevacizumab) when given in combination.
Délai: From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam and palacaparib (+/- bevacizumab) (approx 12 weeks) through 30-day follow-up
|
The plasma concentrations of torvu-sam, total antibody, and total unconjugated payload. |
From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam and palacaparib (+/- bevacizumab) (approx 12 weeks) through 30-day follow-up
|
|
Module 6: Pharmacokinetics of torvu-sam and pembrolizumab (+/- palacaparib) when given in combination.
Délai: From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam and pembrolizumab (+/- palacaparib).(approx 12 weeks) through 90-day follow-up
|
The plasma concentrations of torvu-sam, total antibody, and total unconjugated payload. |
From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam and pembrolizumab (+/- palacaparib).(approx 12 weeks) through 90-day follow-up
|
|
Module 2, 3, 4, 5, and 6: Area Under the concentration-time curve (AUC)
Délai: At predefined intervals throughout the treatment period (approximately 12 weeks)
|
Area under the plasma concentration-time curve |
At predefined intervals throughout the treatment period (approximately 12 weeks)
|
|
Module 2, 3, 4, 5, and 6: Maximum plasma concentration of the study drug (Cmax)
Délai: At predefined intervals throughout the treatment period (approximately 12 weeks)
|
Maximum observed plasma concentration of the study drug |
At predefined intervals throughout the treatment period (approximately 12 weeks)
|
|
Module 2, 3, 4, 5, and 6: Time to maximum plasma concentration of the study drug (T-max)
Délai: At predefined intervals throughout the treatment period (approximately 12 weeks)
|
Time to maximum observed plasma concentration of the study drug |
At predefined intervals throughout the treatment period (approximately 12 weeks)
|
|
Module 2, 3, 4, 5, and 6: Clearance
Délai: At predefined intervals throughout the treatment period (approximately 12 weeks)
|
A pharmacokinetic measurement of the volume of plasma from which the study drug is completely removed per unit time. |
At predefined intervals throughout the treatment period (approximately 12 weeks)
|
|
Module 2, 3, 4, 5, and 6: Terminal elimination half-life (t 1/2)
Délai: From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam (approximately 12 weeks)
|
Terminal elimination half-life. |
From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam (approximately 12 weeks)
|
|
Immunogenicity of torvu-sam
Délai: From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam (approx 2 years) through 30-day follow-up
|
The number and percentage of participants who develop ADAs. |
From the first dose of study intervention, at predefined intervals throughout the administration of torvu-sam (approx 2 years) through 30-day follow-up
|
Collaborateurs et enquêteurs
Parrainer
Les enquêteurs
- Chercheur principal: Funda Meric-Bernstam, MD, UT MD Anderson Cancer Center
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
- Maladies urogénitales
- Maladies génitales
- Maladies du système endocrinien
- Tumeurs urogénitales
- Tumeurs par site
- Tumeurs
- Maladies urogénitales féminines
- Maladies urogénitales féminines et complications de la grossesse
- Tumeurs par type histologique
- Maladies utérines
- Maladies génitales, femme
- Tumeurs des glandes endocrines
- Tumeurs, glandulaires et épithéliales
- Adénocarcinome
- Tumeurs des voies respiratoires
- Tumeurs thoraciques
- Tumeurs pulmonaires
- Maladies ovariennes
- Maladies annexielles
- Tumeurs génitales, femme
- Troubles gonadiques
- Carcinome
- Tumeurs utérines
- Adénocarcinome du poumon
- Tumeurs ovariennes
- Tumeurs de l'endomètre
- Acides aminés, peptides et protéines
- Protéines
- Produits chimiques organiques
- Anticorps, monoclonal, humanisé
- Anticorps, monoclonal
- Anticorps
- Immunoglobulines
- Immunoprotéines
- Protéines sanguines
- Globulines sériques
- Globulines
- Complexes de coordination
- Bévacizumab
- Carboplatine
- pembrolizumab
- AZD5305
Autres numéros d'identification d'étude
- D8990C00001
- 2022-502576-23-00 (Identificateur de registre: CTIS (EU))
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Description du régime IPD
Qualified researchers can request access to anonymized individual patient-level data from AstraZeneca group of companies sponsored clinical trials via the request portal.
All request will be evaluated as per the AZ disclosure commitment:
https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure.
Yes, indicates that AZ are accepting requests for IPD, but this does not mean all requests will be shared.
Délai de partage IPD
AstraZeneca will meet or exceed data availability as per the commitments made to the EFPIA Pharma Data Sharing Principles. For details of our timelines, please rerefer to our disclosure commitment at https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure.
Critères d'accès au partage IPD
When a request has been approved AstraZeneca will provide access to the deidentified individual patient-level data in an approved sponsored tool . Signed Data Sharing Agreement (non-negotiable contract for data accessors) must be in place before accessing requested information. Additionally, all users will need to accept the terms and conditions of the SAS MSE to gain access. For additional details, please review the Disclosure Statements at https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure.
Type d'informations de prise en charge du partage d'IPD
- PROTOCOLE D'ÉTUDE
- SÈVE
Informations sur les médicaments et les dispositifs, documents d'étude
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