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ACTIVE NOT RECRUITINGPhase1

5G-EMERALD: Amivantamab in Malignant Brain Tumours

Sponsor: Institute of Cancer Research, United Kingdom

NCT ID: NCT06632236

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Access to the study treatment being tested
Type of study
Interventional (receives a drug or procedure)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
Amivantamab (drug)
How long the study runs
Study runs about 33 months (dates as stated)
About the drug or intervention
Amivantamab — drug: Amivantamab will be supplied in single-use 350 mg injectable solution, provided as a 7 ml per glass vial (50mg/ml), intended for IV infusion.
Patient visit burden
Not specified by the sponsor
Type of study
Testing a treatment
Ages
16 Years and over
Who
All
Number of participants
12
Started
2024-10-09
Last checked
2026-08

Plain English Summary

What is this study?

  • • Testing a new treatment for malignant primary gliomas
  • • Phase1 - 12 participants
  • • The purpose of this clinical trial is to evaluate the safety and tolerability of amivantamab and to determine the preliminary antitumour activity of amivantamab administered at the recommended Phase 2 dose (RP2D)

Who can take part?

  • • Ages 16 Years and over
  • • Diagnosed with malignant primary gliomas

Where?

  • • Cambridge - Cambridge University Hospitals
  • • Sutton - The Royal Marsden Hospital - Drug Development Unit

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

The purpose of this clinical trial is to evaluate the safety and tolerability of amivantamab and to determine the preliminary antitumour activity of amivantamab administered at the recommended Phase 2 dose (RP2D). In the Phase 1b of this study a biomarker defined arm will be opened, initially in the relapsed GMB setting, enrolling 12 patients. These patients will be treated with amivantamab monotherapy. Amivantamab will be administered intravenously (IV) weekly for the first 4 weeks, then every 2 weeks thereafter until disease progression or unacceptable toxicity. The first dose will be given as a split infusion, 350 mg IV over 4 hours on cycle 1 day 1 and 1400 mg IV over 6 hours on cycle 1 day 2. Subsequent infusions are given at a dose of 1750 mg IV over 2-5 hours in cycle 1 and between 2-3 hours from cycle 2 onwards if the first dose was well-tolerated with no significant toxicity. Progression to Phase 2 is dependent on emergent data and funding.

More detail

The clinical trial will start in Phase 1b (proof of concept of hypothesis-driven biomarker-guided therapies). This is a study within Minderoo 5G: A Next Generation AGile Genomically Guided Glioma Modular Platform for proof-of-concept molecular hypothesis testing in patients with high grade malignant brain tumours. 5G-EMERALD is a Bayesian multi-centre, multi-arm, open-label, adaptive, seamless Phase 1 trial of amivantamab for patients with high grade malignant brain tumours. 5G-EMERALD will recruit patients with glioblastoma (GBM) into one molecularly-defined biomarker arm of patients who have tumours that harbour: • EGFR amplification (high copy number) The above mentioned arm, within Phase 1, will have robust GO/ADAPT decision points, reviewed by the Safety Review Committee (SRC) to allow for both agility and clear direction for next steps. A 2-stage Bayesian adaptive design will be performed to assess preliminary efficacy. In the Phase 1b of this study a biomarker defined arm will be opened, initially in the relapsed GBM setting, enrolling 12 patients onto each arm. These patients will be treated with amivantamab. Amivantamab will be administered intravenously (IV) weekly for the first 4 weeks, then every 2 weeks thereafter until disease progression or unacceptable toxicity.

Malignant Primary GliomasGlioblastoma Multiform (Grade IV Astrocytoma)Diffuse Hemispheric Glioma, H3 G34-MutantGlioblastoma Multiforme (GBM)

How this trial compares with your answers

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What we know so far

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Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 16 Years and over
  • Who can join: All genders

Biomarkers mentioned

have a negativeEGFRserologically positivedemonstrated by positivewith a positiveParticipant is positiveCD4

Treatment history

Treatments you must have had:

  • ✓ to use contraception
  • ✓ to complete antibiotics 1 week
  • ✓ consultation with the Chief Investigator:

What the study is looking for

  • ✓Inclusion Criteria for Phase 1b:
  • ✓Glioblastoma, IDH-wildtype Grade 4
  • ✓Astrocytoma, IDH-mutant, Grade 4 (lower Grade 2/3 are not included)
  • ✓Diffuse hemispheric glioma, H3 G34 mutant Grade 4
  • ✓Patients for Phase 1 will need to have consented to the Minderoo Precision Brain Tumour Programme and have available...
See the full criteria
Inclusion Criteria for Phase 1b: 1. Patients with histologically confirmed advanced WHO Stage IV glioblastoma (per fourth edition 2016). Per the new 2021 fifth edition of WHO Classification of Tumours of the Central Nervous System, this will include: * Glioblastoma, IDH-wildtype Grade 4 * Astrocytoma, IDH-mutant, Grade 4 (lower Grade 2/3 are not included) * Diffuse hemispheric glioma, H3 G34 mutant Grade 4 2. Patients for Phase 1 will need to have consented to the Minderoo Precision Brain Tumour Programme and have available whole genome, and transcriptome data available. 3. Patients for the relapsed cohorts will be eligible at first relapse following completion of optimal surgery, and Stupp based adjuvant chemo-radiotherapy (or equivalent). They will need to have measurable disease per Response Assessment in Neuro-Oncology (RANO) or evaluable disease. 4. Patients for the front line minimal residual disease (MRD) cohort will be eligible following completion of optimal surgery and Stupp based adjuvant chemoradiotherapy as long as they meet all other inclusion/exclusion criteria. 5. 16 years or over. 6. Life expectancy of at least 12 weeks. 7. World Health Organisation (WHO) performance status of 0-1. 8. Neurologically stable (e.g., without a progression of neurological symptoms or requiring escalating doses of systemic steroid therapy within the last week). 9. Written (signed or dated) informed consent and be capable of co-operating with treatment and follow up. 10. Haematological and biochemical indices within the ranges shown below. These measurements must be performed within one week prior to the first dose of either IMP: Haemoglobin (Hb): ≥ 10.0 g/dL Absolute neutrophil count: ≥ 1.5 x 10\^9/L Platelet count: ≥ 75 x 10\^9/L Coagulation: INR \<1.5 and APTT \<1.5x if not anticoagulated INR stable \> 7 days within intended therapeutic range if anticoagulated Bilirubin: ≤ 1.5 x ULN; subjects with Gilbert's syndrome can enrol if conjugated bilirubin is within normal limits. Alanine aminotransferase (ALT) and aspartate aminotransferase (AST): \< 3 x ULN Albumin: ≥ 28 g/L Creatinine: \<1.5 x ULN and creatinine clearance \> 45 ml/min as measured or calculated based on Cockcroft-Gault formula Sodium: ≥ 130 mmol/L Potassium, Calcium, Magnesium, phosphate: Within institution normal ranges (replacement is permitted) Urinary protein: \< 1+ on dipstick 11. Female patients with reproductive potential must have a negative serum, or urine, pregnancy test at screening and within 72 hours of the first dose of study treatment and must agree to further serum or urine pregnancy tests during the study. 12. A participant must be either of the following: a. not of childbearing potential, b. of child-bearing potential and practicing true abstinence during the entire period of the study, including up to 6 months after the last dose of the study treatment is given, or c. of childbearing potential and practicing 2 methods of contraception, including 1 highly effective user independent method and a second method, to avoid impregnating a partner or becoming pregnant, respectively. A participant must agree to continue contraception throughout the study, and for at least 6 months after the last dose of study treatment. Please, refer to section 4.1 of CTFG guidance "Recommendations related to contraception and pregnancy testing in clinical trials" and to section 9.6 of the Master Protocol for further details. Note: If the childbearing potential changes after start of the study (eg, participant of childbearing potential who is not heterosexually active becomes active, premenarchal participant experiences menarche) the participant must begin birth control, as described above. 13. A participant must agree not to donate eggs (ova, oocytes) for the purposes of assisted reproduction during the study and for 6 months after receiving the last dose of study treatment. 14. A participant must wear a condom when engaging in any activity that allows for passage of ejaculate to another person during the study and for 6 months after receiving the last dose of study treatment. A participant who is sexually active with a partner of childbearing potential must agree to use a condom with spermicidal foam/gel/film/cream/suppository and their partner must also be practicing a highly effective method of contraception (ie, established use of oral, injected, or implanted hormonal methods of contraception; placement of an intrauterine device \[IUD\] or intrauterine hormone-releasing system \[IUS\]). If the participant is vasectomized, they must still use a condom (with or without spermicide) for prevention of passage of exposure through ejaculation, but their partner is not required to use contraception. 15. A participant must agree not to donate sperm for the purpose of reproduction during the study and for a minimum of 6 months after receiving the last dose of study treatment. 16. A participant must be willing and able to adhere to the lifestyle restrictions specified in this protocol. Exclusion Criteria for Phase 1b: 1. Receipt of treatment before the first dose of study drug (Cycle 1 Day 1) within an interval shorter than the following, as applicable: * Cytotoxic chemotherapy during the prior 2 weeks or 6 weeks for nitrosoureas * Bevacizumab during the prior 6 weeks * Five half-lives of any small molecule investigational or licensed medicinal product. 2. Prior immune checkpoint inhibitor therapy or vaccine therapy is not permitted. Prior EGFR-targeting therapy is not permitted. Prior use of any other immune-modulatory investigational agent must be discussed with sponsor team and CI. 3. Ongoing Grade 2 or greater toxicities from pre-existing conditions or from previous treatments. 4. Patients with carcinomatous meningitis, leptomeningeal spread of tumour, spread of tumour to the brain stem or spinal cord. 5. Has evidence of recent intratumoural or peritumoural haemorrhage on baseline MRI. Patients with radiological findings that are stable on at least 2 consecutive MRI scans at least 3 weeks apart will be eligible. 6. History of clinically relevant bleeding disorders, including significant gastrointestinal (GI) bleeding within last 6 months. 7. Participant has active cardiovascular disease including, but not limited to: * A medical history of deep venous thrombosis or pulmonary embolism within 1 month prior to first dose of study drug or any of the following within 6 months prior to first dose of study drug: myocardial infarction, unstable angina, stroke, transient ischemic attack, coronary/peripheral artery bypass graft, or any acute coronary syndrome. Clinically non-significant thrombosis such as non-obstructive catheter-associated thrombus, incidental or asymptomatic pulmonary embolism, are not exclusionary. Patients on Warfarin will need to be converted onto low-molecular weight-based heparin therapy. * Participant has a significant genetic predisposition to venous thromboembolic (VTE) events such as Factor V Leiden. * Participant has a prior history of VTE and is not on appropriate therapeutic anticoagulation as per National Comprehensive Cancer Network (NCCN) or local guidelines. * Uncontrolled (persistent) hypertension: systolic blood pressure \> 160 mm Hg; diastolic blood pressure \> 100 mm Hg. * Congestive heart failure (CHF), defined as New York Heart Association (NYHA) class III-IV or hospitalization for CHF (any NYHA class) within 6 months of first dose of the study drug. * Concurrent and clinically significant abnormalities on ECG at Screening, including a corrected QT interval (QTcF \> 460ms). 8. History of malabsorption syndrome or other conditions that may interfere with enteral absorption. Patients with a history of or active inflammatory bowel disease (e.g., Crohn's disease or ulcerative colitis). Patients with acute or chronic pancreatitis. History of GI perforation or fistulae. 9. Has urine protein \> 1g/24 hours. Participants with \> 1+ on urine dipstick testing will undergo 24-hour urine collection for quantitative assessment of proteinuria. 10. Has significant lung disease including pneumonitis, interstitial lung disease (including drug-induced or radiation ILD/pneumonitis), idiopathic pulmonary fibrosis, cystic fibrosis, active tuberculosis, or history of opportunistic infections (including PCP or Cytomegalovirus (CMV) pneumonia). 11. Participant is serologically positive for hepatitis B surface antigen (HbsAg), Note: participants with a prior history of hepatitis B virus (HBV) demonstrated by positive hepatitis B core antibody are eligible if they have at Screening 1) a negative HBsAg and 2) a HBV DNA (viral load) below the lower limit of quantification, per local testing. Subjects with a positive HBsAg due to recent vaccination are eligible if HBV DNA (viral load) is below the lower limit of quantification, per local testing. 12. Participant is serologically positive for hepatitis C antibody. Note: participants with a prior history of hepatitis C virus (HCV), who have completed antiviral treatment and have subsequently documented HCV RNA below the lower limit of quantification per local testing are eligible. 13. Participant has other clinically active infectious liver disease. 14. Participant is positive for human immunodeficiency virus (HIV), with 1 or more of the following: * Receiving antiretroviral therapy (ART) that may interfere with study treatment (consult sponsor for review of medication prior to enrolment). * CD4 count \< 350 at screening * AIDS-defining opportunistic infection within 6 months of start of screening * Not agreeing to start ART and be on ART \> 4 weeks plus having HIV viral load \< 400 copies/mL at end of 4-week period (to ensure ART is tolerated and HIV controlled). 15. Participant has an uncontrolled illness, including but not limited to: * Uncontrolled diabetes * Ongoing or active infection (includes infection requiring treatment with antimicrobial therapy \[participants will be required to complete antibiotics 1 week prior to starting study treatment\] or diagnosed or suspected viral infection. * active bleeding diathesis * Impaired oxygenation requiring continuous oxygen supplementation * Psychiatric illness, social situation, or any other circumstances that would limit compliance with study requirements * Any ophthalmologic condition that is clinically unstable 16. Steroid requirement for neurological symptom control of \> 3mg Dexamethasone per day (patients will allowed to enrol if they have been on a stable dose of steroids of equivalent or less than 3mg Dexamethasone for at least 5 days prior to Day 1 of Cycle 1). 17. Has received a live vaccine within 30 days of planned start of study therapy. Note: inactive vaccines including COVID vaccines are allowed prior to 1 week of Day 1 of Cycle 1). 18. Concurrent or prior malignancy other than the disease under study. The following exceptions require consultation with the Chief Investigator: 1. Non-muscle invasive bladder cancer (NMIBC) treated within the last 24 months that is considered completely cured. 2. Skin cancer (non-melanoma or melanoma) treated within the last 24 months that is completely cured. 3. Non-invasive cervical cancer treated within the last 24 months that is considered completely cured. 19. Is a participant or plans to participate on another interventional clinical trial while taking part in this Phase 1 study. Participation in an observational trial would be acceptable. 20. A participant has major surgery excluding placement of vascular access or tumour biopsy, or had significant traumatic injury within 4 weeks before first dose of study drug or minor surgery within 2 weeks, or will not have fully recovered from surgery, or has surgery planned during the time the participant is expected to participate in the study. Note: Participants with planned surgical procedures to be conducted under local anaesthesia may participate. 21. A participant has palliative radiotherapy within 1 week of the firs dose of study drug, 22. Any other condition which in the investigator's opinion would not make the patient a good candidate for the clinical trial.

Where Is This Study? (2 UK sites)

Cambridge University Hospitals

Cambridge CB2 0QQ, United Kingdom

Hospital R&D contact (matched)

Stephen Kelleher

cuh.research@nhs.net01223 348490

The Royal Marsden Hospital - Drug Development Unit

Sutton SM2 5PT, United Kingdom

Hospital R&D contact (matched)

Mark Brandon-Grove

research.development@rmh.nhs.uk020 3186 5416
Data sourced from ClinicalTrials.gov · Last verified: 2026-08