ClinicalTrials.gg
RecruitingNCT07439094Updated Apr 27, 2026

A First-in-Human Study of CKD-703 in Advanced Solid Tumors and Non-Small Cell Lung Cancer

A Phase 1/2 interventional study of CKD-703 in Advanced Solid Tumors and Non-Small Cell Lung Cancer, sponsored by Chong Kun Dang Pharmaceutical. Recruiting at 1 site in United States. Open to participants aged 19 Years and older. Per ClinicalTrials.gov, last updated 2026-04-27.

Sponsored by Chong Kun Dang Pharmaceutical · Phase 1/2, Interventional, and Treatment

From the registry’s dates

  • Started Apr 2026; still recruiting 6 months later.
Phase
Phase 1/2
Study type
Interventional
Enrollment
140
Allocation
Non-randomized
Ages
19 Years and older
Sex
All
01

Study summary

This is a Phase 1/2a open-label multicenter study to evaluate the safety, efficacy, and pharmacokinetics of CKD-703 in Advanced c-Met Expressing Solid Tumors, and in MET-Amplified and c-Met Overexpressing Non-Small Cell Lung Cancer.

CKD-703 is composed of a c-Met-targeting monoclonal antibody (mAb) coupled to a cytotoxic payload consisting of the anti-microtubule drug monomethyl auristatin E (MMAE); thus, CKD-703 is a novel ADC offering a highly targeted approach with potential improvement of efficacy while reducing off-target effects for patients with NSCLC and other cancers.

02

Conditions studied

  • Advanced Solid Tumors
  • Non-Small Cell Lung Cancer

Keywords

  • c-Met
  • CKD-703
  • Advanced Solid Tumors
  • Non-Small Cell Lung Cancer
03

In context

Carcinoma, Non-Small-Cell Lung

7,620 studies on the registry are indexed under Carcinoma, Non-Small-Cell Lung; 1,838 are open to participants now.

This study's planned enrollment of 140 is above the median of 62 across 6,019 interventional studies indexed under Carcinoma, Non-Small-Cell Lung.

Browse Carcinoma, Non-Small-Cell Lung studies →

Lead sponsor

Chong Kun Dang Pharmaceutical is the lead sponsor of 299 studies on the registry; 15 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
19 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Males and females ≥ 19-year-old
  • Part 1 : Solid tumors including NSCLC for which standard therapy has failed or was not tolerated, and no other effective therapy exists
  • Part 2 : or cytologically documented c-Met overexpressing nonsquamous NSCLC having failed at least 1 line of SoC therapy (platinum-based chemotherapy and/or ).
  • Part 3 : Histologically or cytologically documented c-Met expressing solid tumors for which standard therapy has failed or was not tolerated.
  • In all parts of the study, subjects with NSCLC with documented actionable genetic alterations must have failed at least 1 line of country-level approved targeted therapies
  • ≥ 12 weeks as judged by the Investigator
  • Documented progressive and as defined by 1.1
  • Performance Status 0 or 1

Exclusion criteria

Exclusion Criteria:

  • Subject has received radiation therapy to the lung \< 6 months prior to the first dose of study drug
  • Prior radiotherapy to ≥ 25% of bone marrow
  • Anticancer systemic therapy such as immunotherapy, biologic, cytotoxic chemotherapy, or any therapy (including cell therapy or gene therapy) within a period of 28 days prior to the first dose of study drug. Any anticancer therapy small molecule (eg. kinase inhibitor) or herbal therapy within 14 days prior to the first dose of study drug
  • Prior c-Met-targeted antibody therapy or any MMAE-containing ADC (prior c-Met targeting small molecules are allowed)
  • Use of strong P-gp and/or /5 inducers within 21 days prior or strong P-gp and/or CYP3A4/5 inhibitors within 14 days prior to the first dose of study drug
  • Use of sensitive CYP3A4/5 substrate within 3 days or 5 times half-life prior to the first dose of study drug.
  • Evidence of pulmonary fibrosis on screening imaging assessment or any history of pneumonitis that required treatment with systemic within 12 months of the planned first dose of the study drug
  • History of drug induced interstitial lung disease
  • Prior or active ocular or corneal disease based on ophthalmic evaluation (slit lamp and visual acuity)
  • Prior Grade 3 neuropathy or chronic Grade 2 neuropathy
Terms in these criteria, in plain language(9)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Histologically or cytologically confirmed

The diagnosis was confirmed by looking at a sample under a microscope: tissue from a biopsy or surgery (histology), or cells from a fluid or needle sample (cytology).

Your pathology report is the document that shows this.

PD-1, PD-L1 and checkpoint inhibitors

PD-1, PD-L1 and CTLA-4 are proteins that act as brakes on the immune system. Checkpoint inhibitors, such as pembrolizumab or nivolumab, block them so the immune system can attack a cancer.

PD-L1 can also be measured in a tumour sample. Some scores count stained tumour cells only (TPS); others also count certain immune cells (CPS). The study names the score and the minimum it uses.

Life expectancy

The study doctor’s estimate of how long someone is likely to live. Criteria use it so that people can stay in the study long enough for it to answer its question.

Measurable disease

The amount of disease can be tracked with a defined measurement, so the study can see whether it shrinks or grows. It might be a tumour measured on a scan or, in some blood cancers such as myeloma, a marker measured in blood or urine.

The criteria or the study team say which measurement counts — having no tumour visible on a scan does not by itself rule you out.

RECIST

The standard rules for measuring tumours on CT or MRI scans, to tell whether a cancer is shrinking, stable or growing during treatment.

“Measurable disease per RECIST 1.1” usually means at least one tumour 10 mm or more at its longest on a CT scan, or a lymph node 15 mm or more across its short axis.

ECOG performance status

A scale of how much an illness limits everyday activity. For people being assessed to join a study, scores run from 0 (fully active) to 4; lower is more active.

0
Fully active, no restrictions.
1
Limited in strenuous activity, but walking and able to do light work, such as housework or office work.
2
Walking and able to look after yourself, but unable to work; up and about more than half of waking hours.
3
Able to look after yourself only in part; in bed or a chair more than half of waking hours.
4
Unable to look after yourself at all; in bed or a chair all day.

Studies most often ask for 0–1 or 0–2. Your doctor gives the score; the WHO scale uses the same steps. The full scale also has 5, which records death.

Investigational drug or device

A drug or device being studied in a clinical trial.

It may be new, or already approved and being studied for another use, dose or form. Criteria often leave out people who took part in another study of one within a recent period, commonly 30 days or five half-lives.

CYP3A (CYP3A4) inhibitors and inducers

CYP3A is a group of enzymes, mainly CYP3A4, in the liver and gut that break down many medicines. Some medicines, supplements and foods (grapefruit, St John’s wort) slow them down or speed them up, which changes how much of a study drug stays in the body.

Studies list them so they can be avoided or switched; bring a list of everything you take, including supplements.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

05

Study design

Phase
Phase 1 / Phase 2
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Sequential assignment
Masking
None (open label)
Enrollment
140 participants (estimated)

Study arms

  • Experimental
    Part 1

    Participants with advanced solid tumors will receive escalating dose of CKD-703

    Drug: CKD-703

  • Experimental
    Part 2

    Participants with nsqNSCLC will receive CKD-703

    Drug: CKD-703

  • Experimental
    Part 3

    Participants with advanced solid tumors will receive CKD-703

    Drug: CKD-703

Interventions

  • DrugCKD-703

    Intravenous (IV) Infusion

06

What researchers measure

Primary outcomes

  1. Part 1: Number of patients with dose limiting toxicity (DLT)

    Collect all adverse events at each visit

    Time frame: first 21-day period of therapy

  2. Part 2 and Part 3: Object Response Rate (ORR)

    ORR defined as the proportion of subjects with a best Investigator-assessed confirmed objective response of CR or PR according to RECIST 1.1

    Time frame: Up to 24 months

Secondary outcomes

  1. All parts : Treatment-Emergent Adverse Events (TEAE)

    Incidence of SAEs, SUSARs, TEAEs, and AESI

    Time frame: Up to 24 months

  2. All parts : Immunogenicity (ADA)

    Blood samples were collected and assessed by validated immunoassays for immunogenicity of CKD-703, including the incidence of anti-drug antibodies (ADA)

    Time frame: Up to 24 months

  3. All parts : Immunogenicity (NAb)

    Blood samples were collected and assessed by validated immunoassays for immunogenicity of CKD-703, including the incidence of neutralizing antibodies (NAb)

    Time frame: Up to 24 months

  4. Part 1 and Part 2 : Pharmacokinetic parameter

    CKD-703 (conjugated antibody)

    Time frame: Up to 24 months

  5. Part 1 and Part 2 : Pharmacokinetic parameter

    Total antibody

    Time frame: Up to 24 months

  6. Part 1 and Part 2 : Pharmacokinetic parameter

    Free MMAE

    Time frame: Up to 24 months

  7. Part 1 and Part 3 : Best Overall Response (BOR)

    Defined as best objective response of CR, PR, SD, PD, or not evaluable at the end of treatment

    Time frame: Up to 24 months

  8. All parts : Duration of Response (DoR)

    Defined as the time from the date of first documented CR or PR until the date of documented progression or death

    Time frame: Up to 24 months

  9. Part 2 and Part 3 : Progression-Free Survival (PFS)

    Defined as the time from the date of first dose to the date of progression or death

    Time frame: Up to 24 months

  10. Part 2 and Part 3 : Overall Survival (OS)

    Defined as the time from first dose to the date of death

    Time frame: Up to 24 months

07

Study locations

1 of 1 sites recruiting
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Apr 2026 (actual). Primary completion is estimated for Dec 2029, 44 months after the start.

Of 308 industry-sponsored phase 1/2 interventional studies under Carcinoma, Non-Small-Cell Lung, half reached primary completion within 58 months of starting (the median), counting those still running; a quarter within 39 and three quarters within 77. This study's planned 44 months is below that.

Counting every sponsor, half of 431 studies reached it within 63 months; a quarter within 42 and three quarters within 80.

How these figures are worked out, and which studies are left out of them.

Registered
Feb 13, 2026
First posted
Feb 27, 2026
StartActual
Apr 16, 2026
Primary completionEst.
Dec 2029
CompletionEst.
Dec 2029
Last update
Apr 27, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Apr 27, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07439094
Responsible party
Sponsor
First posted
Feb 27, 2026
Start date
Apr 16, 2026
Primary completion
Dec 2029 (estimated)
Completion
Dec 2029 (estimated)
Last update
Apr 27, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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No contact was published for this record. The registry link below has the sponsor’s details.

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