ClinicalTrials.gg
RecruitingNCT07805369Updated Oct 28, 2026

A Phase 1 Study of DEM301 in Participants With Metastatic Colorectal Cancer

A Phase 1 interventional study of DEM301 in Metastatic Colorectal Cancer, Colon Cancer and Rectal Cancer, sponsored by DEM BioPharma, Inc.. Recruiting at 2 sites in Australia. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-10-28.

Sponsored by DEM BioPharma, Inc. · Phase 1, Interventional, and Treatment

Updated Oct 28, 2026Now RecruitingFirst site in Australia+2 moreGo to Updates ↓
Phase
Phase 1
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

This is a first-in-human Phase 1 study of DEM301 in adults with previously treated advanced metastatic colorectal cancer. DEM301 is an investigational antibody-drug conjugate. The study will evaluate the safety and tolerability of DEM301, identify doses for further study, and assess how the drug behaves in the body and whether it shows signs of activity against the cancer.

Read the detailed description

This is a Phase 1, multicenter, open-label study of DEM301 in participants with previously treated advanced metastatic colorectal cancer. The study has two parts: Dose Escalation, and Dose Expansion.

Dose Escalation will evaluate the safety and tolerability of DEM301 and identify one or more recommended doses for further study. Dose Expansion will further evaluate DEM301 at the selected dose or doses.

The study will also assess preliminary antitumor activity, pharmacokinetics, immunogenicity, pharmacodynamic effects, and exploratory biomarkers. Approximately 60 participants are planned.

02

Conditions studied

  • Metastatic Colorectal Cancer
  • Colon Cancer
  • Rectal Cancer

Keywords

  • DEM301
  • antibody-drug conjugate (ADC)
  • ADC
  • metastatic colorectal cancer (mCRC)
  • mCRC
  • colon cancer
  • rectal cancer
03

In context

Colorectal Neoplasms

6,541 studies on the registry are indexed under Colorectal Neoplasms; 1,667 are open to participants now.

This study's planned enrollment of 60 is below the median of 76 across 4,800 interventional studies indexed under Colorectal Neoplasms.

Browse Colorectal Neoplasms studies →

Lead sponsor

This is the only study on the registry with DEM BioPharma, Inc. as lead sponsor.

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

04

Who can participate

Ages eligible
18 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

  1. Age ≥18 years.
  2. Participants must have documented advanced ( or unresectable) colorectal cancer that has progressed on or after prior standard-of-care treatment and must have received, or been unable to receive, applicable standard therapies as defined in the protocol.
  3. ≥12 weeks.
  4. (ECOG) performance status 0-1.
  5. Have at least 1 at baseline suitable for repeat imaging evaluation by v1.1.
  6. Adequate bone marrow, liver, kidney, and coagulation function per protocol requirements.
  7. Agree to provide adequate tumor tissue for protocol-required biomarker assessment. Participants in designated cohorts must be willing to provide fresh tumor , unless medically .
  8. Female participants must not be pregnant or breastfeeding. Male and female participants must comply with protocol-defined reproductive and requirements.
  9. Have suitable venous access for study treatment and required blood sampling.
  10. Be willing and able to comply with study assessments, schedule, and restrictions.
  11. Written must be obtained before any study-related procedures are performed.

Exclusion criteria

Exclusion Criteria:

  1. Prior treatment with certain antibody-drug conjugates, as defined in the protocol. Protocol-defined exceptions may apply.
  2. Recent anticancer therapy, treatment, major surgery, or radiation therapy within the protocol-defined .
  3. Ongoing toxicity from prior therapy that has not recovered to the protocol-required level.
  4. Active central nervous system (CNS) or suspected or confirmed . Participants with treated and stable may be eligible.
  5. Recent thromboembolic event or clinically significant cardiovascular disease.
  6. Active or uncontrolled infection, including active viral hepatitis, unless protocol-defined eligibility criteria are met.
  7. Known infection or AIDS-related illness unless protocol-defined eligibility criteria are met.
  8. History of or current drug-induced interstitial lung disease/pneumonitis, suspected interstitial lung disease (ILD)/pneumonitis, or other severe or uncontrolled chronic pulmonary disease.
  9. Another within the previous 3 years, except certain malignancies with a low risk of recurrence.
  10. Recent systemic therapy or , except as permitted by the protocol.
  11. Known to DEM301 or its ingredients, or any serious medical, psychiatric, or other condition that, in the Investigator's opinion, could affect participant safety, study participation, or interpretation of study results.
Terms in these criteria, in plain language(19)

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.

Metastases

Cancer that has spread from where it began to other parts of the body. “Metastatic” cancer is cancer that has spread this way.

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.

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.

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.

Biopsy and archival tissue

A biopsy takes a small piece of tissue to examine. “Archival tissue” is a sample already taken, for example at diagnosis, and kept by the hospital.

Whether a stored sample will do depends on when it was taken, how much there is and what the study needs. Ask whether the study accepts your stored sample or needs a new biopsy.

Contraindication

A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.

Contraception

Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.

Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

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.

Washout period

A planned gap after a treatment, so that its effects can lessen before the study treatment or a study assessment. Ask the study team and the doctor who prescribed it before changing any medicine.

Clinically significant

Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.

Leptomeningeal disease

Cancer that has spread to the leptomeninges, the thin layers covering the brain and spinal cord, and the fluid between them. It is not the same as brain metastases.

Criteria often treat it separately, and many studies leave it out even where treated brain metastases are allowed.

Brain metastases

Cancer deposits in the brain from a cancer that started elsewhere in the body (CNS metastases include the spinal cord).

Studies differ: some leave out any brain metastases, some accept ones treated and stable for some weeks. Check what this study allows.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

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.

Live vaccines

Vaccines made with a weakened form of the germ, such as measles–mumps–rubella (MMR), chickenpox and yellow fever. They can be risky when the immune system is weakened. Flu injections are not live; the nasal flu spray is.

Hypersensitivity

An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.

05

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Sequential assignment
Masking
None (open label)
Enrollment
60 participants (estimated)

Study arms

  • Experimental
    Dose Escalation

    Participants will receive DEM301 in sequential Dose Escalation cohorts to evaluate safety and identify doses for further study.

    Drug: DEM301

  • Experimental
    Dose Expansion

    Participants will receive DEM301 at a recommended dose selected based on data from Dose Escalation.

    Drug: DEM301

Interventions

  • DrugDEM301

    DEM301 is an investigational antibody-drug conjugate being evaluated as monotherapy in Dose Escalation and Dose Expansion cohorts.

06

What researchers measure

Primary outcomes

  1. Incidence of Dose-Limiting Toxicities (DLTs)

    Incidence of DLTs in DLT-evaluable participants enrolled in Dose Escalation.

    Time frame: 21 Days

  2. Incidence of Adverse Events (AEs)

    Incidence of AEs, including events requiring dose interruption or discontinuation, in participants enrolled in Dose Escalation and Dose Expansion.

    Time frame: From first dose through 30 days after the last dose, up to approximately 24 months

  3. Incidence of Serious Adverse Events (SAEs)

    Incidence of SAEs in participants enrolled in Dose Escalation and Dose Expansion. Related SAEs occurring after the End of Treatment visit will also be reported according to the protocol.

    Time frame: From signing informed consent through 30 days after the last dose, up to approximately 24 months

Secondary outcomes

  1. Maximum Tolerated Dose (MTD) of DEM301, if Applicable

    The MTD of DEM301, if applicable, will be determined based on available Dose Escalation data.

    Time frame: At completion of Dose Escalation, approximately 12 months

  2. Recommended Dose(s) for Expansion (RDEs) of DEM301

    One or more recommended doses for expansion will be selected based on available Dose Escalation data.

    Time frame: At completion of Dose Escalation, approximately 12 months

  3. Objective Response Rate (ORR) at 12 Weeks

    ORR at 12 weeks will be assessed according to RECIST v1.1 in response-evaluable participants in Dose Escalation and Dose Expansion.

    Time frame: 12 weeks

  4. Duration of Response (DoR)

    Duration of response will be evaluated according to RECIST v1.1 in participants with a documented response in Dose Escalation and Dose Expansion.

    Time frame: Up to approximately 24 months

  5. Disease Control Rate (DCR) at 12 Weeks

    DCR at 12 weeks will be assessed according to RECIST v1.1 in response-evaluable participants in Dose Escalation and Dose Expansion.

    Time frame: 12 Weeks

  6. Progression-Free Survival (PFS) at 12 Weeks

    PFS at 12 weeks will be evaluated in response-evaluable participants in Dose Escalation and Dose Expansion.

    Time frame: 12 Weeks

  7. Overall Survival (OS) at 24 Weeks

    OS at 24 weeks will be evaluated in participants in Dose Escalation and Dose Expansion.

    Time frame: 24 Weeks

  8. Area Under the Concentration-Time Curve (AUC) of DEM301 and Protocol-Specified Analytes

    AUC will be characterized for DEM301 and protocol-specified analytes in participants in Dose Escalation and Dose Expansion.

    Time frame: At protocol-specified pharmacokinetics (PK) sampling time points, up to approximately 24 months

  9. Terminal Elimination Half-Life (t½) of DEM301 and Protocol-Specified Analytes

    Terminal elimination half-life will be characterized for DEM301 and protocol-specified analytes in participants in Dose Escalation and Dose Expansion.

    Time frame: At protocol-specified PK sampling time points, up to approximately 24 months

  10. Maximum Concentration (Cmax) of DEM301 and Protocol-Specified Analytes

    Maximum concentration will be characterized for DEM301 and protocol-specified analytes in participants in Dose Escalation and Dose Expansion.

    Time frame: At protocol-specified PK sampling time points, up to approximately 24 months

  11. Immunogenicity of DEM301

    The presence of anti-drug antibodies and neutralizing antibodies will be evaluated in participants in Dose Escalation and Dose Expansion.

    Time frame: At protocol-specified PK sampling time points, up to approximately 24 months

07

Study locations

2 of 2 sites recruiting
  • Clinical Site 104
    Birtinya, Queensland 4575, Australia
    Recruiting
  • Clinical Site 101
    Nedlands, Western Australia 6009, Australia
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

2 registry updates since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedDate before it movedWhere the date was before it movedSimilar 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

Start is estimated for Oct 2026; primary completion for Sep 2028, 23 months later.

Of 268 industry-sponsored phase 1 interventional studies under Colorectal Neoplasms, half reached primary completion within 47 months of starting (the median), counting those still running; a quarter within 31 and three quarters within 66. This study's planned 23 months is below that.

Counting every sponsor, half of 434 studies reached it within 48 months; a quarter within 31 and three quarters within 69.

Start moved once since we started tracking on Sep 25, 2026: Sep 2026 → Oct 2026, on Oct 15, 2026.

Earlier changes are on the record history on ClinicalTrials.gov ↗

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

Registered
Sep 1, 2026
First posted
Sep 4, 2026
StartEst.
Oct 2026was Sep 2026
Primary completionEst.
Sep 2028
CompletionEst.
Mar 2029
Last update
Oct 28, 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.
Status
Not yet recruiting→Recruiting
changed Oct 15, 2026
Sites
2 sites added — first site in Australia
Show 2 added (2 Australia)
  • Clinical Site 101 · Nedlands, Australia
  • Clinical Site 104 · Birtinya, Australia
across 2 updates, Oct 15, 2026 – Oct 28, 2026
Start date
Sep 2026→Oct 2026
Oct 15, 2026
Show all 2 updates
  1. Oct 28, 2026
    1 site added
    Show site
    • Clinical Site 104 · Birtinya, Australia
  2. Oct 15, 2026
    Not yet recruiting→Recruiting
    1 site added — first site in Australia
    Show site
    • Clinical Site 101 · Nedlands, Australia
    Start date Sep 2026→Oct 2026
    + 1 other change: verification date

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07805369
Lead sponsor
DEM BioPharma, Inc.
Responsible party
Sponsor
First posted
Sep 4, 2026
Start date
Oct 2026 (estimated)
Primary completion
Sep 2028 (estimated)
Completion
Mar 2029 (estimated)
Last update
Oct 28, 2026

Study contacts

DEM301 Study Team
Contact
clinicaltrials@dembiopharma.com
857-242-1002

Oversight

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

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