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AzTrials

NSCLC Patients With EGFR Activating MutationPhase 1NCT07755397

First in Human Multicenter Open Name Dose-increase, Consolidation Method to Study Safety Drug-level in Blood & Drug Metabolism Clinical Activity of Oral JBI-778 in Lung Cancer Patients With, Without Brain Metastasis IDH Mutated WHO Grade 3,4 Recurrent Glioma, Salivary Glands Tumor

A Phase 1 study testing JBI-778 in people with NSCLC Patients With EGFR Activating Mutation and Adenoid Cystic Carcinoma Metastatic, run by Jubilant Therapeutics India Limited at 6 sites in India.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

This is a phase 1, multicentre, first-in-human, open-label, dose-escalation/consolidation study to investigate the safety, pharmacokinetics, pharmacodynamics, and clinical activity of orally administered JBI-778 in EGFR mutated lung cancer patients with or without brain metastasis, IDH mutated WHO grade 3 /4 recurrent… Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
JBI-778
Type of treatment
Pill or oral medicine
Could I receive a placebo?
No, everyone receives an active treatment
How many people
30 participants
Where
6 sitesIndia
Study dates
26 Aug 2024to Apr 2028
Phase
Phase 1
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Male or female participants aged ≥18 years.
  • Histologically or cytologically confirmed:
  • EGFR-mutated non-small cell lung cancer (NSCLC) with or without brain metastases previously treated with an EGFR inhibitor; or
  • IDH-mutated WHO Grade 3/4 recurrent glioma; or
  • Adenoid cystic carcinoma (ACC) with recurrent, metastatic, or advanced incurable disease.
  • At least one measurable lesion according to RECIST v1.1 and/or RANO criteria, as applicable.
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  • ECOG performance status ≤2.
  • Adequate hematologic, hepatic, renal, and coagulation function.
  • Resolution of clinically significant toxicities from prior therapy to Grade 0 or 1, except permitted residual toxicities.
  • Life expectancy of at least 3 months.
  • Able to swallow oral medication.
  • Availability of tumor tissue and/or liquid biopsy suitable for next-generation sequencing.
  • Willing to use highly effective contraception during study participation and for at least 3 months after the last dose of study treatment.
  • Able and willing to provide written informed consent.

Who cannot join

  • Systemic anticancer therapy or investigational therapy within 2 weeks or 5 half-lives prior to study treatment.
  • Major surgery within 21 days before study treatment.
  • Radiotherapy within 4 weeks for brain metastases or within 2 weeks for other disease sites.
  • Significant uncontrolled cardiovascular, metabolic, psychiatric, or other serious medical conditions.
  • QTcF >450 msec in males or >470 msec in females.
  • History of optic neuritis or optic neuropathy.
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  • Active HIV infection or active hepatitis B or C infection.
  • Active infection requiring systemic antibiotic therapy.
  • Use of strong CYP3A inhibitors or inducers within protocol-specified washout periods.
  • Gastrointestinal conditions that may significantly affect drug absorption.
  • Pregnancy or breastfeeding.
  • Participation in another interventional clinical study.
  • Previous treatment with JBI-778.
  • Any condition that, in the opinion of the investigator, would place the participant at unacceptable risk or interfere with study participation.

Trial locations and contacts

6 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Kumar Prabhash contact

+919167760576

kprabhash1@gmail.com

6 sites in 1 country

India6 sites, 6 recruiting
  • Oncoville Cancer Hospital and Research Center

    Bangalore, Karnataka, 560072

    Recruiting
  • Tata Memorial Center

    Mumbai, Maharashtra, 400012

    Recruiting
  • HCG Manavata Cancer Centre

    Nashik, Maharashtra, 422002

    Recruiting
  • All India Institute of Medical Sciences(AIIMS)

    New Delhi, National Capital Territory of Delhi, 110029

    Recruiting
  • Kiran Super Multi-Speciality Hospital

    Surat, Gujarat, 395004

    Recruiting
  • SunAct Cancer Institute Pvt Ltd

    Thane, Maharashtra, 400615

    Recruiting

Other trials in India

About this study

Official title: A Phase 1, Multicenter, Open-Label, Dose-Escalation/Consolidation Study to Investigate the Safety, Pharmacokinetics, Pharmacodynamics and Clinical Activity of Orally Administered JBI-778 in EGFR Mutated Lung Cancer Patients With or Without Brain Metastasis, Isocitrate Dehydrogenase (IDH) Mutated WHO Grade 3/4 Recurrent Glioma and Adenoid Cystic Carcinoma (ACC)

This is a phase 1, multicentre, first-in-human, open-label, dose-escalation/consolidation study to investigate the safety, pharmacokinetics, pharmacodynamics, and clinical activity of orally administered JBI-778 in EGFR mutated lung cancer patients with or without brain metastasis, IDH mutated WHO grade 3 /4 recurrent glioma and ACC with evidence of recurrent, metastatic or advanced, incurable disease arising from any primary site. A total of 42 patients will be recruited in the study. The initial dose escalation up to cohort 3 (estimate to be 160mg) or until the pharmacologically active dose is reached, whichever comes first as determined by the safety committee will be performed only in EGFR mutant NSCLC patients with or without stable cerebral metastases and ACC patients. Once this dose level is reached IDH mutant WHO grade 3 /4 glioma patients will be added. Once the RP2D is determined following dose escalation, additional patients, up to 12, will be treated at that dose to obtain further safety data and preliminary efficacy. Approximately 4 to 6 sites are anticipated for the dose-escalation/consolidation, additional sites will be evaluated as needed. Study will be initiated only after receipt of regulatory and ethics committee (EC) approval. After signing the informed consent form, the patients will undergo screening assessments to confirm eligibility. Eligible patients will be considered first for initial dose escalation and once the RP2D is determined following dose escalation, additional patients, up to 12, will be treated at that dose to obtain further safety data and preliminary efficacy. The RP2D will be establish after a detailed analysis of the totality of dose escalation data, including PK, safety, efficacy, CNS penetration based on CSF sample for study drug presence, analysis of PD markers in peripheral blood and both pre-treatment and on treatment tumor biopsies.

The duration of participation for each patient will be as follows: Screening: - Up to 21 days (-21 to 1 days); Treatment period: Treatment cycle of 21-day each. Treatment may continue for up to 2 years from the start of treatment, provided that the patient experiences clinical benefit in the opinion of the Investigator and shows no signs or symptoms of unequivocal progression of the disease, unacceptable toxicity, or other reasons for study discontinuation. End of treatment (EOT)/ Early termination (ET) visit Safety Follow-up: 30 days after last dose Survival: Every 3 months

Read the detailed description

Dose-Escalation:

The initial dose escalation up to cohort 3 (estimate to be 160mg) or until the pharmacologically active dose is reached, whichever comes first as determined by the safety committee will be performed only in EGFR mutant NSCLC patients with or without stable cerebral metastases and ACC patients. Once this dose level is reached IDH mutated WHO grade 3 /4 glioma patients will be added. The starting dose of JBI-778 is 40 mg orally, once daily in 21-day treatment cycles using a 3+3 design. Dose escalation will be 100% until dose level 3 (i.e., 160 mg) afterwards, a maximum of 33%-75% dose increment will be implemented (up to 75% dose increment if no dose limiting toxicity (DLT), but 33% dose increment if one DLT is observed in the previous dose level, applicable to any dose level not just after 160mg), rounded up or down based on capsule strength. With these restrictions, the next dose to be studied will be determined by the sponsor with approval by the Safety Review Committee (SRC). In the event that any DLTs occur at the starting dose in 2 patients, and with the approval of the SRC, a 20 mg once daily dose level will be evaluated using a 3+3 design. If 20 mg once daily is not tolerated, no further patients will be recruited, and the study will be terminated. In addition to the PK evaluation, patients in dose-escalation will provide pre-treatment and on treatment tissue and/or liquid biopsies to aid in the assessment.

In the 3+3 design, if 3 patients at a dose level complete the DLT evaluation period with no DLT, that dose level of JBI-778 will be deemed safe, and another 3 patients will be treated at the next higher dose level. If 1 of the first 3 patients experience a DLT, 3 more patients will be treated at the same JBI-778 dose level. If 2 or more of the 3 to 6 patients in any dose level experience a DLT, dosing will stop at that level, and either the previous dose level will be considered the Maximum Tolerated Dose (MTD) or intermediate doses may be explored to determine MTD, especially if the difference between the non-tolerated dose and the previous dose is > 50%.

Dose-escalation will continue until any of the following events occur:

  • The highest planned dose level is determined to be safe and tolerable (Minimum of 6 DLT evaluable patients).
  • An MTD is identified. Additional dose levels may be explored based on emerging data (Additional patients (up to 6 patients may be enrolled in 1 or more dose levels that have been shown to be safe and tolerable, defined as backfill enrolment). This backfill enrolment will be done to better estimate the RP2D and to better characterize the safety, efficacy, PK and pharmacodynamics (PD) for JBI 778 and may be concurrent with dose-escalation to identify the MTD. Study patients who do not complete the DLT period for reasons other than study drug toxicity will be replaced. All patients will be assessed for a response using relevant RECIST 1.1 and RANO criteria. Clinical status will be assessed by the NANO instrument. Intra-patient dose-escalations are allowed in this study. Patients who complete the DLT period, tolerate the dose, and have been on the treatment for ≥ 2 cycles without significant toxicities may proceed to a higher dose level for the following treatment cycle if the next dose cohort is deemed safe (For both acute and cumulative toxicities) at that time by the Safety Review Committee (SRC), and after consultation with the Sponsor if the patient has not experienced any ≥ Grade 2 adverse events (deemed treatment-related by the Investigator) during entire prior treatment. The maximum Intra-patient Dose-Escalation level should be one level below the current actively enrolling dose level if tolerability based on the protocol defined criteria have not yet been established. Patients who do not proceed to a higher dose may continue to receive additional cycles at their original dose, based on the decision of the investigator and concurrence by the SRC. An SRC will have oversight of safety and will meet at the end of each cohort and approximately quarterly and as needed during the dose-escalation phase to review cumulative toxicity data, make recommendations to the Sponsor regarding ongoing safety and dose-escalations. The SRC may recommend protocol amendments to maintain patient safety at any stage. In addition, any serious adverse events (SAEs) will be forwarded to the SRC upon occurrence. Safety and tolerability of JBI-778 will be characterized by adverse event and serious adverse event type, severity (graded using the National Cancer Institute Common Terminology Criteria for Adverse Events [NCI CTCAE] Version 5.0), timing, and relationship to study therapy, and laboratory abnormalities in the first and in subsequent cycles. Administration of JBI-778 may continue until evidence of disease progression, intolerance to study medication, or withdrawal of consent. Stable or responding patients who experience DLTs may continue therapy once DLTs have resolved.
Being tested
JBI-778

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • JBI-778Drug

    JBI-778 is an orally administered selective PRMT5 inhibitor supplied as capsules. The starting dose is 40 mg once daily. Participants will receive JBI-778 in continuous 21-day treatment cycles with dose escalation based on a 3+3 design. Capsules are taken orally with water approximately 1 hour before a meal or 2 hours after a meal.

Study groups in NCT07755397
Study groupRoleWhat they receive
JBI-778 Dose EscalationExperimentalParticipants will receive orally administered JBI-778 once daily in continuous 21-day treatment cycles. Dose escalation will follow a 3+3 design beginning at 40 mg daily to determine the maximum tolerated dose (MTD) and recommended Phase 2 dose (RP2D). Additional participants may be enrolled at the RP2D to further evaluate safety, pharmacokinetics, pharmacodynamics, and preliminary antitumor activity.
Receives: Drug: JBI-778

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Incidence of Dose-Limiting Toxicities (DLTs)

    Incidence of dose-limiting toxicities during the DLT evaluation period to determine the maximum tolerated dose (MTD) and recommended Phase 2 dose (RP2D) of JBI-778.

    Measured: At the end of Cycle 1 (each cycle is 21 days)

Secondary outcomes (6)
  1. Incidence of Treatment-Emergent Adverse Events (TEAEs)

    Number of participants with treatment-emergent adverse events, classified by system organ class and severity according to NCI CTCAE v5.0.

    Measured: Up to 2 years

  2. Maximum Plasma Concentration (Cmax) of JBI-778

    Maximum observed plasma concentration of JBI-802 following dosing. Units: ng/mL

    Measured: From Cycle 1 Day 1 up to Cycle 2 Day 1 (each cycle is 21 days)

  3. Area Under the Plasma Concentration-Time Curve (AUC0-t) of JBI-778

    Area under the plasma concentration-time curve from time 0 to last measurable concentration.

    Measured: From Cycle 1 Day 1 up to Cycle 2 Day 1 (each cycle is 21 days)

  4. Time to Maximum Plasma Concentration (Tmax) of JBI-802

    Time to reach maximum plasma concentration.

    Measured: From Cycle 1 Day 1 up to Cycle 2 Day 1 (each cycle is 21 days)

  5. Progression-Free Survival (PFS)

    Progression-free survival in months assessed according to RECIST v1.1 and/or RANO criteria as applicable.

    Measured: up to 2years

  6. Change in Symmetric Dimethylarginine (SDMA)

    Change from baseline in SDMA concentration as a pharmacodynamic marker of PRMT5 inhibition.

    Measured: Up to 2 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted10 Aug 2026
  2. Study start26 Aug 2024
  3. Primary completionMar 2028 (estimated)
  4. Study completionApr 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 1
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
30 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07755397
Sponsor's protocol ID
JBI-778_101
Other IDs
CTRI/2024/07/070802
Status last verified
Aug 2026
First submitted
5 Aug 2026
Last updated
10 Aug 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A Phase 1 study testing JBI-778 in people with NSCLC Patients With EGFR Activating Mutation and Adenoid Cystic Carcinoma Metastatic, run by Jubilant Therapeutics India Limited at 6 sites in India.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 14 inclusion and 14 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 10 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 6 sites in India. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Kumar Prabhash (+919167760576, kprabhash1@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Incidence of Dose-Limiting Toxicities (DLTs) (time frame: At the end of Cycle 1 (each cycle is 21 days)). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Aug 2026.

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