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Experimental drug targets dangerous calcium spike in cancer

NCT ID NCT04198480

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early This study
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Sep 18, 2026 · Last updated Sep 18, 2026

Summary

Researchers are testing an experimental drug called JMT103 in adults with cancer whose blood calcium levels are dangerously high and who have not responded to standard intravenous bisphosphonate treatment. Participants receive JMT103 as an injection under the skin every four weeks, with extra loading doses in the first two weeks. The trial measures whether the drug can bring corrected serum calcium down to a safer level within 10 days of the first dose. This is a small, early-phase study designed to assess both safety and potential benefit.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
JMT103, an experimental injectable drug
What this could lead to
If it works, JMT103 could offer a new option for cancer patients whose high blood calcium no longer responds to standard intravenous bisphosphonates.
What could go wrong
This is a very small, early-stage trial with only a handful of participants, so results may not hold up in larger studies. JMT103 is experimental, and its safety and effectiveness in this setting are not yet established.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Phase 1/2

Runs two stages together: safety and dose first, then whether the treatment works.

Participants

4 people

The number who actually took part.

Started

Apr 2020

Finished

Oct 2021

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: 1. Fully informed and signed informed consent. 2. Male or female, Adults (\>/=18 years). 3. Hypercalcemia of Malignancy (HCM) as defined as documented histologically or cytologically confirmed cancer and a corrected serum calcium (CSC) \> 12.5 mg/dL (3.1 mmol /L). 4. Last IV bisphosphonate treatment must be \>/= 7 days and \</= 30 days before the screening corrected serum calcium; or Last hydration therapy must be \>/= 24 hours before the screening corrected serum calcium(Incompatible bisphosphonate). 5. Adequate organ function. Exclusion Criteria: 1. Pregnancy. 2. Hyperparathyroidism, or other granulomatous disease. 3. Hepatitis b surface antigen positive. 4. Hepatitis c antibody positive, or HIV antibody positive. 5. Receiving dialysis for renal failure. 6. Known sensitivity to JMT103 composition. 7. Treatment with thiazides, calcitonin, mithramycin, or gallium nitrate within their window of expected therapeutic effect (as determined by the physician) prior to the date of screening CSC. 8. Treatment with cinacalcet within 4 weeks prior to the date of screening CSC. 9. Currently participating another clinical study,or Four weeks or less since receiving an investigational product in another clinical study. 10. In the opinion of the investigator , being unsuitable for inclusion in the study,or subjects withdraw informed consent. 11. Treatment with monoclonal antibody to RANK ligand (RANKL) within 180 days prior to the date of the screening CSC.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Shanghai East Hospital

    Shanghai, 200123, China