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Could a common bone drug help fight a rare cancer?

NCT ID NCT03173976

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 This study
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
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This status has not been confirmed recently, so it may be out of date.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 Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This phase 1b trial is testing whether giving zoledronic acid, a drug usually used for bone thinning, before surgery can help people with chondrosarcoma, a rare bone cancer. Seventeen adults with any grade of the disease that can be surgically removed will receive the drug and then have their tumors assessed for changes. The main goals are to check safety and see if the drug affects tumor cells and bone damage.

What this could mean

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

Active substance
Zoledronic acid (a bone-strengthening drug)
What this could lead to
If it works, this could point toward a new way to shrink or control chondrosarcoma tumors before surgery, potentially improving outcomes.
What could go wrong
This is a very early, small phase 1 trial with only 17 people, so results may not apply broadly. The drug may cause side effects like kidney issues or jaw problems, and it's not yet known if it truly helps patients.

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

The first testing in people. Mainly checks safety and dose, usually in a small group.

Participants

17 people

The number who actually took part.

Started

Jul 2017

Expected to finish

May 2028

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

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. Male or female patients aged \>/= 18 years old 2. ECOG Performance Status of \</= 2 3. Written informed consent from subject or the subject's legally authorized representative, obtained prior to participation in the study and any related procedures being performed 4. Patients must meet the following laboratory criteria: 1. Hematology: * Neutrophil count of \>1500/mm * Platelet count of \> 100,000/mm3 * Hemoglobin \&#8805; 9 g/dL 2. Biochemistry: * AST/SGOT and ALT/SGPT \</=2.5 x upper limit of normal (ULN) or \</=5.0 x ULN if the transaminase elevation is due to disease involvement * Serum bilirubin \</= 1.5 x ULN; for subjects with Gilbert's syndrome, direct bilirubin \</=1.5×ULN and indirect bilirubin \</=3×ULN * Serum creatinine \</= 1.5 x ULN or estimated creatinine clearance \>/= 50 ml/min by Cockcroft-Gault equation: GFR=(140-age)\*(wt in kg)\*(0.85 if female)/(72xCr) * Total serum calcium (corrected for serum albumin) \>/= 8.5 mg/dL or ionized calcium \>/= 3.8 mg/dL * Serum potassium \>/= LLN * Serum sodium \>/= LLN * Serum albumin \>/= 3g/dl 5. Any patient with a biopsy proven diagnosis of chondrosarcoma that is grade I, II or III or in cases where histological and radiological correlation suggests low grade chondrosarcoma as per multidisciplinary discussion. 6. Patients with biopsy proven dedifferentiated chondrosarcoma that chose not to pursue neoadjuvant chemotherapy are allowed. 7. Patients must not have received zoledronic acid (ZA) for any reason prior to the study. 8. Patients with metastatic disease are allowed, if indication to remove primary tumor. Exclusion criteria 1. Prior use of Osteoclast inhibitors for osteoporosis within 6 months from screening will not be allowed. 2. Impaired cardiac function 3. Uncontrolled hypertension 4. Creatinine \>1.5 or history of Renal disease preventing use of ZA. 5. Other concurrent severe and/or uncontrolled medical conditions including need for urgent dentoalveolar surgery as indicated by preventative dental exam 6. Concomitant use of any anti-cancer therapy or radiation therapy 7. Women who are pregnant or breast feeding or WOCBP not willing to use a double barrier method of contraception during the study and 3 months after the end of treatment. One of these methods of contraception must be a barrier method. WOCBP are defined as sexually mature women who have not undergone a hysterectomy or who have not been naturally postmenopausal for at least 12 consecutive months (i.e., who has had menses any time in the preceding 12 consecutive months).

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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

  • University of Iowa Hospitals and Clinics

    Iowa City, Iowa, 52242, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.