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.
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
- Conditions the study is for
- NSCLC Patients With EGFR Activating Mutation, Adenoid Cystic Carcinoma Metastatic, Adenoid Cystic Carcinoma of the Head and Neck
- 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.
6 sites in 1 country
India6 sites, 6 recruiting
- 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
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.
- Conditions
- NSCLC Patients With EGFR Activating Mutation, Adenoid Cystic Carcinoma Metastatic, Adenoid Cystic Carcinoma of the Head and Neck
- 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 group | Role | What they receive |
|---|---|---|
| JBI-778 Dose Escalation | Experimental | Participants 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.
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)
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
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)
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)
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)
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
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.
- First posted10 Aug 2026
- Study start26 Aug 2024
- Primary completionMar 2028 (estimated)
- Study completionApr 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for NSCLC Patients With EGFR Activating MutationStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Jubilant Therapeutics India Limited
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
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
Study at a glance
From the registry record, last updated by the sponsor on 10 Aug 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- 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)
- ClinicalTrials.gov ID
- NCT07755397
- Acronym / sponsor ID
- JBI-778_101
- Conditions
- NSCLC Patients With EGFR Activating Mutation, Adenoid Cystic Carcinoma Metastatic, Adenoid Cystic Carcinoma of the Head and Neck
- Phase
- Phase 1
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 30 participants (estimated)
- Lead sponsor
- Jubilant Therapeutics India LimitedIndustry (pharma, biotech, devices)
- Study start
- 26 Aug 2024 (actual)
- Primary completion
- Mar 2028 (estimated)
- Study completion
- Apr 2028 (estimated)
- First posted
- 10 Aug 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| JBI-778 Dose Escalation | Experimental | Drug: JBI-778Participants 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. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (14 listed)
- Male or female participants aged ≥18 years.
- Histologically or cytologically confirmed:
- At least one measurable lesion according to RECIST v1.1 and/or RANO criteria, as applicable.
- ECOG performance status ≤2.
- Adequate hematologic, hepatic, renal, and coagulation function.
Key exclusion criteria (14 listed)
- 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.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| JBI-778JBI-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. | Drug | JBI-778 Dose Escalation |
Primary outcome
Incidence of Dose-Limiting Toxicities (DLTs)
Time frame: At the end of Cycle 1 (each cycle is 21 days)
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.
6 secondary outcomes
Incidence of Treatment-Emergent Adverse Events (TEAEs)
Time frame: Up to 2 years
Maximum Plasma Concentration (Cmax) of JBI-778
Time frame: From Cycle 1 Day 1 up to Cycle 2 Day 1 (each cycle is 21 days)
Area Under the Plasma Concentration-Time Curve (AUC0-t) of JBI-778
Time frame: From Cycle 1 Day 1 up to Cycle 2 Day 1 (each cycle is 21 days)
Time to Maximum Plasma Concentration (Tmax) of JBI-802
Time frame: From Cycle 1 Day 1 up to Cycle 2 Day 1 (each cycle is 21 days)
Progression-Free Survival (PFS)
Time frame: up to 2years
Change in Symmetric Dimethylarginine (SDMA)
Time frame: Up to 2 years
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 10 Aug 2026.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
6 sites in 1 country: see every site and its status.
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.