Advanced Solid TumorPhase 1/2NCT05933265
Study of LP-184 in Patients With Advanced Solid Tumors
A Phase 1/2 study testing LP-184, Olaparib and Nivolumab & Ipilimumab in people with Advanced Solid Tumor and Metastatic Solid Tumor, run by Lantern Pharma Inc. at 7 sites in United States.
Trial summary
The primary objective of this study is to evaluate the safety, tolerability, MTD and RP2D of LP-184 in patients with advanced solid tumors who have relapsed from or are refractory to standard therapy or for whom no standard therapy is available. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Advanced Solid Tumor, Metastatic Solid Tumor, GBM
- What is being tested?
- LP-184, Olaparib and Nivolumab & Ipilimumab
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 64 participants
- Where
- 7 sitesUnited States
- Study dates
- 9 Jun 2023to 28 Jul 2026
- Phase
- Phase 1/2
- 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
Patient Inclusion Criteria:
- ≥18 years of age at the time of consent
- Provided signed written ICF and voluntary consent prior to any mandatory study-specific procedures, sampling, and analyses.
- Have a histologically or cytologically documented advanced solid tumor that has relapsed from or is refractory to standard treatment, or for which no standard treatment is available. Note: patients with certain tumor types such as those with relatively high prevalence of DDR gene alterations and/or PTGR1 over expression (e.g., triple negative breast cancer, lung, prostate, ovarian, pancreatic, bladder, and GBM) may be preferentially enrolled in Phase 1a.
- ECOG performance status 0-1 or Karnofsky performance scale >60 for GBM patients.
- Patients must have measurable disease per RECIST 1.1 or RANO 2.0 criteria as applicable. Note: patients without measurable disease may be eligible, following discussion with the investigator and the sponsor, if the patient presents with non-measurable but evaluable disease of any size unequivocally attributable to advanced solid tumor.
- Patients must have life expectancy >3 months.
- Adequate organ function at screening defined as: Liver Function
- AST, ALT ≤3 x ULN or <5 x ULN in cases of documented liver metastases or involvement of liver in the disease process.
- Total serum bilirubin ≤1.5 x ULN or <5 x ULN if secondary to Gilbert's syndrome or documented liver metastases or involvement of liver in the disease process. Renal Function
- Serum creatinine clearance ≥60 mL/min either measured or calculated using standard Cockcroft-Gault formula.
- Serum electrolyte (potassium, calcium, and magnesium) levels within the normal reference range (may be supplemented according to institutional standard). Bone Marrow Function:
- ANC ≥1500/μL.
- Hemoglobin ≥8 g/dL (The use of transfusion or other intervention to achieve hemoglobin ≥8 g/dL is acceptable. For those patients undergoing RBC transfusion, hemoglobin must be evaluated at least 14 days after the last RBC transfusion).
- Platelet count ≥100,000/μL (assessed ≥7 days following last platelet transfusion in patients with thrombocytopenia requiring platelets). Blood clotting function:
- INR and aPTT ≤1.5 x ULN. Study patients on therapeutic doses of anticoagulation medication must have INR and/or aPTT ≤ the upper limit of the therapeutic range for intended use.
- Women of childbearing potential (WOCBP) must have a negative serum or urine pregnancy test within 3 days of first dose of LP-184. A woman is of child-bearing potential unless she:
- has had a hysterectomy, bilateral tubal ligation, or bilateral oophorectomy;
- is age ≥60 years and is amenorrhoeic; or
- is age <60 years and has been amenorrhoeic for ≥12 months (including no irregular menses or spotting) in the absence of any medication which induces a menopausal state and has documented ovarian failure by serum estradiol and follicle-stimulating hormone levels within the institutional laboratory postmenopausal range).
- WOCBP or must agree to use highly effective contraceptive methods and avoid egg donation during the study treatment and for 6 months after the last dose of LP-184.
- Men of reproductive potential agree to use highly effective contraceptive methods and avoid sperm donation during the study treatment and for 3 months after the last dose of LP-184. A man is of child-producing potential unless he has had a bilateral vasectomy with documented aspermia or a bilateral orchiectomy.
- Is willing to provide archived samples (blocks and/or slides) for comprehensive DDR genomic analyses and/or PTGR1 expression profiling and/or other genomic alterations if the patient has a PR/CR.
- Regarding brain metastases, based on screening contrast brain MRI, patients must have 1of the following:
- No evidence of brain metastases
- Untreated brain metastases not requiring immediate local therapy. For patients with untreated CNS lesions >2.0 cm on screening contrast brain MRI, discussion with and approval from the Medical Monitor is required prior to enrollment.
- Previously treated brain metastases that are either stable for at least 4 weeks since last treatment or progressed since prior local CNS therapy and not requiring immediate re-treatment with local therapy in the opinion of the investigator.
Patient Exclusion Criteria:
- Exposure to anti-cancer therapy within 2 weeks or within at least 5 half-lives of the anticancer agent whichever is shorter; or 4 weeks from any biologics/immunotherapies or any investigational therapy prior to the first dose of LP-184. Note: Low dose steroids (oral prednisone or equivalent ≤20 mg/day, except patients with GBM), localized non-CNS radiotherapy, previous hormonal therapy with luteinizing hormone-releasing hormone agonists for prostate cancer and treatment with bisphosphonates and RANKL inhibitors are not criteria for exclusion if such therapy has not been changed within 4 weeks before LP-184 treatment.
- Any history of retinopathy and/or macular degeneration (without specifications or grades).
- Has received radiation within 4 weeks of Cycle 1 Day 1. Unless the tumor at the site of treatment continues to increase in size after the patient has completed radiotherapy treatment.
- Infection requiring antibiotics, antivirals, or antifungals within 1 week prior to first dose of study drug, unless such infection is adequately controlled (defined as exhibiting no ongoing signs/symptoms related to the infection and with clinical improvement). In the case of prophylactic use of these agents, discussion with the Medical Monitor is required prior to enrollment.
- Hepatitis B and/or hepatitis C infection (as detected by positive testing for hepatitis B surface antigen [HbsAg] or antibody to hepatitis C virus with confirmatory testing) or known seropositivity for or history of active viral infection with human immunodeficiency virus (HIV).
- Are pregnant or breastfeeding. (NOTE: breast milk cannot be stored for future use while the mother is being treated on study).
- Have clinically significant cardiac disease including:
- New York Heart Association Class IV heart failure.
- Myocardial infarction or stroke ≤3 months prior to the first dose of LP-184.
- Unstable angina within ≤12 weeks prior to the first dose of LP-184 unless the underlying disease has been corrected by procedural intervention e.g., stent, bypass.
- Severe aortic stenosis.
- Uncontrolled arrhythmia. Sponsor approval of patients with arrhythmia is required.
- QTc >470 ms by Fredericia criteria.
- Congenital long QT syndrome, or a QT interval corrected by Fridericia's formula (QTcF) >470 ms (average of triplicate ECGs) at Screening and/or on Cycle 1 Day 1 (pre-dose) except for a documented bundle branch block or unless secondary to pacemaker. In the case of a documented bundle branch block or a pacemaker, discussion with the medical monitor is required prior to enrollment.
- Have clinically significant AEs that have not returned to baseline or ≤Grade 1 based on NCI-CTCAE prior to first dose of study drug, unless approved by the sponsor. Patients with chronic Grade 2 toxicities may be eligible per the discretion of the investigator and sponsor (e.g., Grade 2 chemotherapy-induced neuropathy, alopecia, or hypothyroidism from prior immunotherapy treatment).
- Have had major surgery (requiring general anesthesia) within ≤4 weeks of first dose of LP-184.
- Have any other serious medical condition which, in the opinion of the investigator, would preclude the patient from study participation.
- Have clinically active brain metastases, defined as untreated and symptomatic, or requiring therapy with steroids at a dose > 2 mg of dexamethasone or equivalent or anticonvulsants to control associated symptoms. Patients with treated brain metastases that are no longer symptomatic and who require no treatment with steroids may be included in the study if they have recovered from the acute toxic effect of radiotherapy. A minimum of 4 weeks must have elapsed between the end of whole brain radiotherapy and study enrollment (1 week for stereotactic radiotherapy).
- For patients with suspected or known CNS metastatic disease, based on screening brain MRI, patients must not have: Any untreated brain lesions >2.0 cm in size unless Medical Monitor approved enrollment. Ongoing use of systemic corticosteroids for control of symptoms of brain metastases at a total daily dose of >2 mg of dexamethasone (or equivalent). Patients on a chronic stable dose of ≤2 mg total daily of dexamethasone (or equivalent) are eligible with discussion and approval by the medical monitor. (Note: this is not applicable to patients with GBM). Any brain lesion thought to require immediate local therapy, including (but not limited to) a lesion in an anatomic site where an increase in size or possible treatment-related edema may pose a risk to the patient (e.g., brain stem lesions). Patients who underwent local treatment for such lesions identified by screening contrast brain MRI may still be eligible based on criteria described under CNS inclusion criteria described above.
- Known or suspected leptomeningeal disease as documented by the investigator.
- Male patients with partners currently pregnant, or male patients able to father children, and female patients of childbearing potential who are unwilling or unable to use highly effective methods of contraception as outlined in this protocol for the duration of the study and for at least 3 months (male) or 6 months (female) after last dose of study drug
Trial locations and contacts
7 sites in 1 country.
7 sites in 1 country
United States7 sites
John Hopkins - The Sidney Kimmel Comprehensive Cancer Center
Baltimore, Maryland, 21287
Indiana University Melvin and Bren Simon Cancer Center
Indianapolis, Indiana, 46202
Norton Healthcare, Inc.
Louisville, Kentucky, 40205
Fox Chase Cancer Center
Philadelphia, Pennsylvania, 19111
UT Health Science Center San Antonio
San Antonio, Texas, 78229
Highlands Oncology Group
Springdale, Arkansas, 72758
START Mountain Region
West Valley City, Utah, 84119
About this study
Official title: A Phase 1/2 Dose Escalation and Cohort Expansion Study of LP-184 in Patients With Advanced or Metastatic Solid Tumors
The primary objective of this study is to evaluate the safety, tolerability, MTD and RP2D of LP-184 in patients with advanced solid tumors who have relapsed from or are refractory to standard therapy or for whom no standard therapy is available. The secondary objectives are to characterize the PK of LP-184 and its metabolites in plasma and assess clinical activity of LP-184.
Participants will receive LP-184 infusion during Day 1 and Day 8 of each 21-day cycle, for a minimum of two cycles. Patients will be monitored for safety, PK, and clinical activity
Read the detailed description
Patients who meet all eligibility criteria will be enrolled to receive treatment with LP-184 at a dose determined based on the available cohort at the time of each patient's enrollment. Patients will receive LP-184 infusion during Day 1 and Day 8 of each 21-day cycle, for a minimum of two cycles. Patients will be monitored for safety, PK, and clinical activity. Dose escalation is planned with minimum of 3 patient cohorts (starting at dose level 1). After selection of the maximum tolerated dose (MTD), additional patients will be enrolled at two dose levels, including the MTD, as determined by the Safety Review Committee, until at least 10 patients each are treated at each dose to determine the recommended phase 2 dose.
- Conditions
- Advanced Solid Tumor, Metastatic Solid Tumor, GBM, TNBC - Triple-Negative Breast Cancer, NSCLC, Pancreatic Adenocarcinoma
- Being tested
- LP-184, Olaparib, Nivolumab & Ipilimumab
- Keywords
- LP-184, Phase 1, Lantern Pharma, Cancer, DNA damage repair
- Medical subject headings
- Neoplasm Metastasis, Triple Negative Breast Neoplasms, Neoplasms
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
LP-184Drug
LP-184 is a small molecule alkylating agent causing tumor cell death through DNA damage.
OlaparibDrug
A poly (ADP-ribose) polymerase (PARP) inhibitor that impairs homologous recombination (HR) dependent DNA damage repair by trapping PARP1/2 on DNA, leading to synthetic lethality in BRCA1/2-deficient cells.
Nivolumab & IpilimumabDrug
Nivolumab is monoclonal antibody and classified as an immune checkpoint inhibitor. By blocking the PD-1 receptor on the surface of T cells, Nivolumab restores immune cells' ability to recognize and attack cancer cells.
Ipilimumab is monoclonal antibody and classified as an immune checkpoint inhibitor. By blocking the CTLA4 protein on the surface of T cells, Ipilimumab activates T-cells and allows T-cells to attack cancer cells.
| Study group | Role | What they receive |
|---|---|---|
| Master Protocol | Experimental | A phase 1/2 dose escalation and cohort expansion study of LP-184 in patients with advanced or metastatic solid tumors. A BOIN design will be used to evaluate the safety of LP-184, determine the MTD, and identify the RP2D. Patients who meet all eligibility criteria will be enrolled to receive treatment with LP-184 at a dose determined based on the available cohort at the time of each patient's enrollment. Patients will receive LP-184 infusion during Day 1 and Day 8 of each 21-day cycle, for a minimum of two cycles. Receives: Drug: LP-184 |
| Supplement A | Experimental | Phase 1b/2 Expansion cohort of participants with triple negative breast cancer (TNBC), non-small cell lung cancer (NSCLC), pancreatic adenocarcinoma (PDAC) or other solid tumours with known DDR genomic alterations to determine the optimal dose/RP2D and to obtain preliminary estimates of clinical activity. Receives: Drug: LP-184 |
| Supplement C | Experimental | Phase 1b/2 Expansion cohort of participants with Hormone Receptor (HR)-Negative and HER2-Negative Breast Cancer (TNBC) to evaluate the safety, tolerability and clinical activity of LP-184 in combination with olaparib Receives: Drug: LP-184; Drug: Olaparib |
| Supplement D | Experimental | Phase 1b/2 Expansion cohort of participants with KEAP1 and/or STK11-mutated and programmed cell death ligand-1 (PD-L1)-low NSCLC to evaluate the safety, tolerability and clinical activity of LP-184 in combination with nivolumab and ipilimumab in . Receives: Drug: LP-184; Drug: Nivolumab & Ipilimumab |
What is being measured
The primary outcome is the main question the study is designed to answer.
To evaluate the safety and tolerability of LP-184 assessed by the incidence and severity of all adverse events graded by CTCAE v5.0
Measured: 12 months
To determine the MTD of LP-184 based on all available safety (graded by CTCAE v5.0) and PK data.
Measured: 12 months
To determine the RP2D of LP-184 based on all available safety (graded by CTCAE v5.0), PK, PD and efficacy data
Measured: 12 months
Secondary outcomes (6)
To characterize the PK of LP-184 and its metabolites in plasma by assessing the area under the plasma concentration versus time curve (AUC).
Measured: Blood samples for PK analysis collected at multiple time points during cycle 1 (each cycle is 21 days)
To characterize the PK of LP-184 and its metabolites in plasma by assessing the peak plasma concentration (Cmax)
Measured: Blood samples for PK analysis collected at multiple time points during cycle 1 (each cycle is 21 days)
To characterize the PK of LP-184 and its metabolites in plasma by assessing the time to peak plasma concentration (Tmax)
Measured: Blood samples for PK analysis collected at multiple time points during cycle 1 (each cycle is 21 days)
To characterize the PK of LP-184 and its metabolites in plasma by assessing the amount of time required for the drug concentration in plasma to be reduced to exactly half its starting concentration (half-life, t1/2)
Measured: Blood samples for PK analysis collected at multiple time points during cycle 1 (each cycle is 21 days)
To characterize the PK of LP-184 and its metabolites in plasma by assessing the apparent volume of distribution at steady state after non-intravenous administration (Vss/F)
Measured: Blood samples for PK analysis collected at multiple time points during cycle 1 (each cycle is 21 days)
To assess the clinical activity of LP-184. Overall response rates defined as percentage of patients with CR or PR per RECIST 1.1 or RANO 2.0 criteria in Gliomas
Measured: Tumor imaging is obtained every 6 weeks or 2 cycles (each cycle being 21 days long) for the first 5 cycles and every 12 weeks or 4 cycles unless increased frequency is clinically indicated up to 1 year
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted6 Jul 2023
- Study start9 Jun 2023
- Primary completion28 Jul 2026 (estimated)
- Study completion28 Jul 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (3)Papers the sponsor has linked to this study.
- Other trials for Advanced Solid TumorStudies 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 1/2
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Sequential
- Model description
- BOIN Design
- Masking
- None (open label)
- Enrolment
- 64 participants (actual)
Sponsor and investigators
- Lead sponsor
- Lantern Pharma Inc.
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Reggie Ewesuedo, MD, Study director, Lantern Pharma Inc.
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05933265
- Sponsor's protocol ID
- LTRN184-1AST23-1
- Status last verified
- Apr 2026
- First submitted
- 23 Jun 2023
- Last updated
- 4 May 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Schreck KC, Lal B, Zhou J, Lopez-Bertoni H, Holdhoff M, Ewesuedo R, Bhatia K, Chamberlain M, Laterra J. Phase Ia Evaluation of LP-184 in Recurrent Glioblastoma: Safety, Pharmacokinetics, and Translational Optimization of CNS Exposure. Cancer Res Commun. 2026 Oct 1;6(10):2519-2528. doi: 10.1158/2767-9764.CRC-26-0518.
PubMed 42849034Zhou J, Mahadevan D, Parekh J, Chamberlain M, Bhatia K, Ewesuedo R. Quantitative characterization of platelet count and alanine aminotransferase dynamics to inform personalized dosing in the first-in-human LP-184 trial. Cancer Chemother Pharmacol. 2026 Aug 12;96(1):88. doi: 10.1007/s00280-026-04937-2.
PubMed 42581203Mahadevan D, Parekh J, Beck JT, McKean WB Jr, Schreck KC, Olszanski AJ, Shields MD, Phan V, Hamm JT, Bank BB, Zhou J, Chamberlain M, Bhatia K, Ewesuedo R. A first-in-human phase 1a study of LP-184, a tumor-site activated novel alkylating agent, in patients with advanced solid tumors. Invest New Drugs. 2026 Jul 7. doi: 10.1007/s10637-026-01626-y. Online ahead of print.
PubMed 42410111
Study at a glance
From the registry record, last updated by the sponsor on 4 May 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Phase 1/2 Dose Escalation and Cohort Expansion Study of LP-184 in Patients With Advanced or Metastatic Solid Tumors
- ClinicalTrials.gov ID
- NCT05933265
- Acronym / sponsor ID
- LTRN184-1AST23-1
- Conditions
- Advanced Solid Tumor, Metastatic Solid Tumor, GBM, TNBC - Triple-Negative Breast Cancer, NSCLC, Pancreatic Adenocarcinoma
- Keywords
- LP-184, Phase 1, Lantern Pharma, Cancer, DNA damage repair
- Phase
- Phase 1/2
- Study type
- Interventional
- Recruitment status
- Active, not recruiting
- Enrolment
- 64 participants (actual)
- Lead sponsor
- Lantern Pharma Inc.Industry (pharma, biotech, devices)
- Study start
- 9 Jun 2023 (actual)
- Primary completion
- 28 Jul 2026 (estimated)
- Study completion
- 28 Jul 2026 (estimated)
- First posted
- 6 Jul 2023 (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.
The primary objective of this study is to evaluate the safety, tolerability, MTD and RP2D of LP-184 in patients with advanced solid tumors who have relapsed from or are refractory to standard therapy or for whom no standard therapy is available. The secondary objectives are to characterize the PK of LP-184 and its metabolites in plasma and assess clinical activity of LP-184.
Participants will receive LP-184 infusion during Day 1 and Day 8 of each 21-day cycle, for a minimum of two cycles. Patients will be monitored for safety, PK, and clinical activity
Detailed description
Patients who meet all eligibility criteria will be enrolled to receive treatment with LP-184 at a dose determined based on the available cohort at the time of each patient's enrollment. Patients will receive LP-184 infusion during Day 1 and Day 8 of each 21-day cycle, for a minimum of two cycles. Patients will be monitored for safety, PK, and clinical activity. Dose escalation is planned with minimum of 3 patient cohorts (starting at dose level 1). After selection of the maximum tolerated dose (MTD), additional patients will be enrolled at two dose levels, including the MTD, as determined by the Safety Review Committee, until at least 10 patients each are treated at each dose to determine the recommended phase 2 dose.
Study design
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Sequential
- Masking
- None (open label)
- Number of arms
- 4
- Model description
- BOIN Design
| Arm | Type | Receives |
|---|---|---|
| Master Protocol | Experimental | Drug: LP-184A phase 1/2 dose escalation and cohort expansion study of LP-184 in patients with advanced or metastatic solid tumors. A BOIN design will be used to evaluate the safety of LP-184, determine the MTD, and identify the RP2D. Patients who meet all eligibility criteria will be enrolled to receive treatment with LP-184 at a dose determined based on the available cohort at the time of each patient's enrollment. Patients will receive LP-184 infusion during Day 1 and Day 8 of each 21-day cycle, for a minimum of two cycles. |
| Supplement A | Experimental | Drug: LP-184Phase 1b/2 Expansion cohort of participants with triple negative breast cancer (TNBC), non-small cell lung cancer (NSCLC), pancreatic adenocarcinoma (PDAC) or other solid tumours with known DDR genomic alterations to determine the optimal dose/RP2D and to obtain preliminary estimates of clinical activity. |
| Supplement C | Experimental | Drug: LP-184, Drug: OlaparibPhase 1b/2 Expansion cohort of participants with Hormone Receptor (HR)-Negative and HER2-Negative Breast Cancer (TNBC) to evaluate the safety, tolerability and clinical activity of LP-184 in combination with olaparib |
| Supplement D | Experimental | Drug: LP-184, Drug: Nivolumab & IpilimumabPhase 1b/2 Expansion cohort of participants with KEAP1 and/or STK11-mutated and programmed cell death ligand-1 (PD-L1)-low NSCLC to evaluate the safety, tolerability and clinical activity of LP-184 in combination with nivolumab and ipilimumab in . |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
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 |
|---|---|---|
| LP-184LP-184 is a small molecule alkylating agent causing tumor cell death through DNA damage. | Drug | Master Protocol, Supplement A, Supplement C, Supplement D |
| OlaparibA poly (ADP-ribose) polymerase (PARP) inhibitor that impairs homologous recombination (HR) dependent DNA damage repair by trapping PARP1/2 on DNA, leading to synthetic lethality in BRCA1/2-deficient cells. | Drug | Supplement C |
| Nivolumab & IpilimumabNivolumab is monoclonal antibody and classified as an immune checkpoint inhibitor. By blocking the PD-1 receptor on the surface of T cells, Nivolumab restores immune cells' ability to recognize and attack cancer cells. Ipilimumab is monoclonal antibody and classified as an immune checkpoint inhibitor. By blocking the CTLA4 protein on the surface of T cells, Ipilimumab activates T-cells and allows T-cells to attack cancer cells. | Drug | Supplement D |
Primary outcome
To evaluate the safety and tolerability of LP-184 assessed by the incidence and severity of all adverse events graded by CTCAE v5.0
Time frame: 12 months
To determine the MTD of LP-184 based on all available safety (graded by CTCAE v5.0) and PK data.
Time frame: 12 months
To determine the RP2D of LP-184 based on all available safety (graded by CTCAE v5.0), PK, PD and efficacy data
Time frame: 12 months
6 secondary outcomes
To characterize the PK of LP-184 and its metabolites in plasma by assessing the area under the plasma concentration versus time curve (AUC).
Time frame: Blood samples for PK analysis collected at multiple time points during cycle 1 (each cycle is 21 days)
To characterize the PK of LP-184 and its metabolites in plasma by assessing the peak plasma concentration (Cmax)
Time frame: Blood samples for PK analysis collected at multiple time points during cycle 1 (each cycle is 21 days)
To characterize the PK of LP-184 and its metabolites in plasma by assessing the time to peak plasma concentration (Tmax)
Time frame: Blood samples for PK analysis collected at multiple time points during cycle 1 (each cycle is 21 days)
To characterize the PK of LP-184 and its metabolites in plasma by assessing the amount of time required for the drug concentration in plasma to be reduced to exactly half its starting concentration (half-life, t1/2)
Time frame: Blood samples for PK analysis collected at multiple time points during cycle 1 (each cycle is 21 days)
To characterize the PK of LP-184 and its metabolites in plasma by assessing the apparent volume of distribution at steady state after non-intravenous administration (Vss/F)
Time frame: Blood samples for PK analysis collected at multiple time points during cycle 1 (each cycle is 21 days)
To assess the clinical activity of LP-184. Overall response rates defined as percentage of patients with CR or PR per RECIST 1.1 or RANO 2.0 criteria in Gliomas
Time frame: Tumor imaging is obtained every 6 weeks or 2 cycles (each cycle being 21 days long) for the first 5 cycles and every 12 weeks or 4 cycles unless increased frequency is clinically indicated up to 1 year
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 4 May 2026.
- Derived from this study: PubMed 42849034Schreck KC, Lal B, Zhou J, Lopez-Bertoni H, Holdhoff M, Ewesuedo R, Bhatia K, Chamberlain M, Laterra J. Phase Ia Evaluation of LP-184 in Recurrent Glioblastoma: Safety, Pharmacokinetics, and Translational Optimization of CNS Exposure. Cancer Res Commun. 2026 Oct 1;6(10):2519-2528. doi: 10.1158/2767-9764.CRC-26-0518.
- Derived from this study: PubMed 42581203Zhou J, Mahadevan D, Parekh J, Chamberlain M, Bhatia K, Ewesuedo R. Quantitative characterization of platelet count and alanine aminotransferase dynamics to inform personalized dosing in the first-in-human LP-184 trial. Cancer Chemother Pharmacol. 2026 Aug 12;96(1):88. doi: 10.1007/s00280-026-04937-2.
- Derived from this study: PubMed 42410111Mahadevan D, Parekh J, Beck JT, McKean WB Jr, Schreck KC, Olszanski AJ, Shields MD, Phan V, Hamm JT, Bank BB, Zhou J, Chamberlain M, Bhatia K, Ewesuedo R. A first-in-human phase 1a study of LP-184, a tumor-site activated novel alkylating agent, in patients with advanced solid tumors. Invest New Drugs. 2026 Jul 7. doi: 10.1007/s10637-026-01626-y. Online ahead of print.
- Individual participant dataSharing planned: No
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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. This study is not recruiting at the moment.
Reggie Ewesuedo, MD study director
Lantern Pharma Inc.
7 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 1/2 study testing LP-184, Olaparib and Nivolumab & Ipilimumab in people with Advanced Solid Tumor and Metastatic Solid Tumor, run by Lantern Pharma Inc. at 7 sites in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
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: under way, not looking for participants, as of the sponsor's last update on 4 May 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 7 sites in United States. 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 combined 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.
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
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?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
To evaluate the safety and tolerability of LP-184 assessed by the incidence and severity of all adverse events graded by CTCAE v5.0 (time frame: 12 months). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT05933265, which also lists 3 linked publications.
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 4 May 2026.