Abraxane

Neoplasm Metastasis, refractory Testicular germ cell cancer, advanced Thymoma + 19 more

Treatment

11 FDA approvals

20 Active Studies for Abraxane

What is Abraxane

Paclitaxel

The Generic name of this drug

Treatment Summary

Paclitaxel, sold under the brand name Taxol, is a chemotherapy drug used to treat various cancers. It was first discovered in the bark of the Pacific yew tree in 1971 and is available as an intravenous solution or the newer formulation Abraxane, which contains albumin-bound paclitaxel. Paclitaxel works by inhibiting cell growth and division, preventing cancer cells from multiplying.

Paclitaxel

is the brand name

image of different drug pills on a surface

Abraxane Overview & Background

Brand Name

Generic Name

First FDA Approval

How many FDA approvals?

Paclitaxel

Paclitaxel

2001

60

Approved as Treatment by the FDA

Paclitaxel, also known as Paclitaxel, is approved by the FDA for 11 uses which include Non-Small Cell Lung Carcinoma (NSCLC) and Metastatic Non-Small Cell Lung Cancer .

Non-Small Cell Lung Carcinoma (NSCLC)

Used to treat Non-Small Cell Lung Carcinoma (NSCLC) in combination with Cisplatin

Metastatic Non-Small Cell Lung Cancer

Used to treat Metastatic Non-Small Cell Lung Cancer in combination with Carboplatin

Advanced Ovarian Cancer

Used to treat Advanced Ovarian Cancer in combination with Cisplatin

Metastatic Breast Cancer

Pancreatic Adenocarcinoma Metastatic

Used to treat Pancreatic Adenocarcinoma Metastatic in combination with Gemcitabine

Neoplasm Metastasis

Used to treat Pancreatic Adenocarcinoma Metastatic in combination with Gemcitabine

Carcinoma, Non-Small-Cell Lung

Used to treat Locally Advanced Non-Small Cell Lung Cancer in combination with Carboplatin

Malignant Neoplasms

Used to treat Metastatic Non-Small Cell Lung Cancer in combination with Carboplatin

Non-Small Cell Lung Cancer

Used to treat Non-Small Cell Lung Carcinoma (NSCLC) in combination with Cisplatin

Metastatic Breast Cancer

Ovarian Neoplasms

Used to treat Advanced Ovarian Cancer in combination with Cisplatin

Effectiveness

How Abraxane Affects Patients

Paclitaxel is an antineoplastic agent typically used to treat ovarian cancer, breast cancer, and other types of cancer. Paclitaxel works by forming and stabilizing microtubules in cells, which stops the normal reorganization of microtubules that are needed for cell functions. This can lead to the formation of abnormal microtubule structures during cell division.

How Abraxane works in the body

Paclitaxel disrupts the normal functioning of microtubules, which are an important part of a cell's structure. Paclitaxel binds to the beta subunit of tubulin, which makes up microtubules, and prevents them from disassembling. This makes it difficult for the cell to move molecules around, which is essential for cell functioning. Paclitaxel also binds to a protein called Bcl-2, which stops programmed cell death, and prevents it from working. This leads to cell death in cancer cells.

When to interrupt dosage

The portion of Abraxane is contingent upon the determined condition, including advanced Soft Tissue Sarcoma (STS), Malignant Neoplasms and Ovarian Cancer. The measure of dosage can be found in the table below, depending on the method of delivery (e.g. Liquid - Intravenous or Injection, solution - Intravenous).

Condition

Dosage

Administration

Sarcoma

, 10.0 mg/mL, 30.0 mg/mL, 6.0 mg/mL, 100.0 mg, 5.0 mg/mL, 60.0 mg

, Intravenous, Injection, Injection - Intravenous, Injection, solution, concentrate, Injection, solution, concentrate - Intravenous, Injection, solution, Injection, solution - Intravenous, Injection, powder, lyophilized, for suspension - Intravenous, Injection, powder, lyophilized, for suspension, Solution - Intravenous, Solution, Powder, for suspension, Powder, for suspension - Intravenous, Liquid - Intravenous, Liquid, Injection, powder, for suspension, Injection, powder, for suspension - Intravenous, Injection, powder, for solution, Injection, powder, for solution - Intravenous

refractory Testicular germ cell cancer

, 10.0 mg/mL, 30.0 mg/mL, 6.0 mg/mL, 100.0 mg, 5.0 mg/mL, 60.0 mg

, Intravenous, Injection, Injection - Intravenous, Injection, solution, concentrate, Injection, solution, concentrate - Intravenous, Injection, solution, Injection, solution - Intravenous, Injection, powder, lyophilized, for suspension - Intravenous, Injection, powder, lyophilized, for suspension, Solution - Intravenous, Solution, Powder, for suspension, Powder, for suspension - Intravenous, Liquid - Intravenous, Liquid, Injection, powder, for suspension, Injection, powder, for suspension - Intravenous, Injection, powder, for solution, Injection, powder, for solution - Intravenous

advanced Thymoma

, 10.0 mg/mL, 30.0 mg/mL, 6.0 mg/mL, 100.0 mg, 5.0 mg/mL, 60.0 mg

, Intravenous, Injection, Injection - Intravenous, Injection, solution, concentrate, Injection, solution, concentrate - Intravenous, Injection, solution, Injection, solution - Intravenous, Injection, powder, lyophilized, for suspension - Intravenous, Injection, powder, lyophilized, for suspension, Solution - Intravenous, Solution, Powder, for suspension, Powder, for suspension - Intravenous, Liquid - Intravenous, Liquid, Injection, powder, for suspension, Injection, powder, for suspension - Intravenous, Injection, powder, for solution, Injection, powder, for solution - Intravenous

Non-Small Cell Lung Cancer

, 10.0 mg/mL, 30.0 mg/mL, 6.0 mg/mL, 100.0 mg, 5.0 mg/mL, 60.0 mg

, Intravenous, Injection, Injection - Intravenous, Injection, solution, concentrate, Injection, solution, concentrate - Intravenous, Injection, solution, Injection, solution - Intravenous, Injection, powder, lyophilized, for suspension - Intravenous, Injection, powder, lyophilized, for suspension, Solution - Intravenous, Solution, Powder, for suspension, Powder, for suspension - Intravenous, Liquid - Intravenous, Liquid, Injection, powder, for suspension, Injection, powder, for suspension - Intravenous, Injection, powder, for solution, Injection, powder, for solution - Intravenous

Advance Directives

, 10.0 mg/mL, 30.0 mg/mL, 6.0 mg/mL, 100.0 mg, 5.0 mg/mL, 60.0 mg

, Intravenous, Injection, Injection - Intravenous, Injection, solution, concentrate, Injection, solution, concentrate - Intravenous, Injection, solution, Injection, solution - Intravenous, Injection, powder, lyophilized, for suspension - Intravenous, Injection, powder, lyophilized, for suspension, Solution - Intravenous, Solution, Powder, for suspension, Powder, for suspension - Intravenous, Liquid - Intravenous, Liquid, Injection, powder, for suspension, Injection, powder, for suspension - Intravenous, Injection, powder, for solution, Injection, powder, for solution - Intravenous

Ovarian Cancer

, 10.0 mg/mL, 30.0 mg/mL, 6.0 mg/mL, 100.0 mg, 5.0 mg/mL, 60.0 mg

, Intravenous, Injection, Injection - Intravenous, Injection, solution, concentrate, Injection, solution, concentrate - Intravenous, Injection, solution, Injection, solution - Intravenous, Injection, powder, lyophilized, for suspension - Intravenous, Injection, powder, lyophilized, for suspension, Solution - Intravenous, Solution, Powder, for suspension, Powder, for suspension - Intravenous, Liquid - Intravenous, Liquid, Injection, powder, for suspension, Injection, powder, for suspension - Intravenous, Injection, powder, for solution, Injection, powder, for solution - Intravenous

Ovarian Cancer

, 10.0 mg/mL, 30.0 mg/mL, 6.0 mg/mL, 100.0 mg, 5.0 mg/mL, 60.0 mg

, Intravenous, Injection, Injection - Intravenous, Injection, solution, concentrate, Injection, solution, concentrate - Intravenous, Injection, solution, Injection, solution - Intravenous, Injection, powder, lyophilized, for suspension - Intravenous, Injection, powder, lyophilized, for suspension, Solution - Intravenous, Solution, Powder, for suspension, Powder, for suspension - Intravenous, Liquid - Intravenous, Liquid, Injection, powder, for suspension, Injection, powder, for suspension - Intravenous, Injection, powder, for solution, Injection, powder, for solution - Intravenous

Acquired Immunodeficiency Syndrome

, 10.0 mg/mL, 30.0 mg/mL, 6.0 mg/mL, 100.0 mg, 5.0 mg/mL, 60.0 mg

, Intravenous, Injection, Injection - Intravenous, Injection, solution, concentrate, Injection, solution, concentrate - Intravenous, Injection, solution, Injection, solution - Intravenous, Injection, powder, lyophilized, for suspension - Intravenous, Injection, powder, lyophilized, for suspension, Solution - Intravenous, Solution, Powder, for suspension, Powder, for suspension - Intravenous, Liquid - Intravenous, Liquid, Injection, powder, for suspension, Injection, powder, for suspension - Intravenous, Injection, powder, for solution, Injection, powder, for solution - Intravenous

Urinary Bladder Neoplasms

, 10.0 mg/mL, 30.0 mg/mL, 6.0 mg/mL, 100.0 mg, 5.0 mg/mL, 60.0 mg

, Intravenous, Injection, Injection - Intravenous, Injection, solution, concentrate, Injection, solution, concentrate - Intravenous, Injection, solution, Injection, solution - Intravenous, Injection, powder, lyophilized, for suspension - Intravenous, Injection, powder, lyophilized, for suspension, Solution - Intravenous, Solution, Powder, for suspension, Powder, for suspension - Intravenous, Liquid - Intravenous, Liquid, Injection, powder, for suspension, Injection, powder, for suspension - Intravenous, Injection, powder, for solution, Injection, powder, for solution - Intravenous

Malignant Neoplasms

, 10.0 mg/mL, 30.0 mg/mL, 6.0 mg/mL, 100.0 mg, 5.0 mg/mL, 60.0 mg

, Intravenous, Injection, Injection - Intravenous, Injection, solution, concentrate, Injection, solution, concentrate - Intravenous, Injection, solution, Injection, solution - Intravenous, Injection, powder, lyophilized, for suspension - Intravenous, Injection, powder, lyophilized, for suspension, Solution - Intravenous, Solution, Powder, for suspension, Powder, for suspension - Intravenous, Liquid - Intravenous, Liquid, Injection, powder, for suspension, Injection, powder, for suspension - Intravenous, Injection, powder, for solution, Injection, powder, for solution - Intravenous

Metastatic Melanoma

, 10.0 mg/mL, 30.0 mg/mL, 6.0 mg/mL, 100.0 mg, 5.0 mg/mL, 60.0 mg

, Intravenous, Injection, Injection - Intravenous, Injection, solution, concentrate, Injection, solution, concentrate - Intravenous, Injection, solution, Injection, solution - Intravenous, Injection, powder, lyophilized, for suspension - Intravenous, Injection, powder, lyophilized, for suspension, Solution - Intravenous, Solution, Powder, for suspension, Powder, for suspension - Intravenous, Liquid - Intravenous, Liquid, Injection, powder, for suspension, Injection, powder, for suspension - Intravenous, Injection, powder, for solution, Injection, powder, for solution - Intravenous

Uterine Cervical Neoplasms

, 10.0 mg/mL, 30.0 mg/mL, 6.0 mg/mL, 100.0 mg, 5.0 mg/mL, 60.0 mg

, Intravenous, Injection, Injection - Intravenous, Injection, solution, concentrate, Injection, solution, concentrate - Intravenous, Injection, solution, Injection, solution - Intravenous, Injection, powder, lyophilized, for suspension - Intravenous, Injection, powder, lyophilized, for suspension, Solution - Intravenous, Solution, Powder, for suspension, Powder, for suspension - Intravenous, Liquid - Intravenous, Liquid, Injection, powder, for suspension, Injection, powder, for suspension - Intravenous, Injection, powder, for solution, Injection, powder, for solution - Intravenous

Stomach Cancer

, 10.0 mg/mL, 30.0 mg/mL, 6.0 mg/mL, 100.0 mg, 5.0 mg/mL, 60.0 mg

, Intravenous, Injection, Injection - Intravenous, Injection, solution, concentrate, Injection, solution, concentrate - Intravenous, Injection, solution, Injection, solution - Intravenous, Injection, powder, lyophilized, for suspension - Intravenous, Injection, powder, lyophilized, for suspension, Solution - Intravenous, Solution, Powder, for suspension, Powder, for suspension - Intravenous, Liquid - Intravenous, Liquid, Injection, powder, for suspension, Injection, powder, for suspension - Intravenous, Injection, powder, for solution, Injection, powder, for solution - Intravenous

Peritoneal Neoplasms

, 10.0 mg/mL, 30.0 mg/mL, 6.0 mg/mL, 100.0 mg, 5.0 mg/mL, 60.0 mg

, Intravenous, Injection, Injection - Intravenous, Injection, solution, concentrate, Injection, solution, concentrate - Intravenous, Injection, solution, Injection, solution - Intravenous, Injection, powder, lyophilized, for suspension - Intravenous, Injection, powder, lyophilized, for suspension, Solution - Intravenous, Solution, Powder, for suspension, Powder, for suspension - Intravenous, Liquid - Intravenous, Liquid, Injection, powder, for suspension, Injection, powder, for suspension - Intravenous, Injection, powder, for solution, Injection, powder, for solution - Intravenous

Head and Neck Neoplasms

, 10.0 mg/mL, 30.0 mg/mL, 6.0 mg/mL, 100.0 mg, 5.0 mg/mL, 60.0 mg

, Intravenous, Injection, Injection - Intravenous, Injection, solution, concentrate, Injection, solution, concentrate - Intravenous, Injection, solution, Injection, solution - Intravenous, Injection, powder, lyophilized, for suspension - Intravenous, Injection, powder, lyophilized, for suspension, Solution - Intravenous, Solution, Powder, for suspension, Powder, for suspension - Intravenous, Liquid - Intravenous, Liquid, Injection, powder, for suspension, Injection, powder, for suspension - Intravenous, Injection, powder, for solution, Injection, powder, for solution - Intravenous

Small cell carcinoma of lung

, 10.0 mg/mL, 30.0 mg/mL, 6.0 mg/mL, 100.0 mg, 5.0 mg/mL, 60.0 mg

, Intravenous, Injection, Injection - Intravenous, Injection, solution, concentrate, Injection, solution, concentrate - Intravenous, Injection, solution, Injection, solution - Intravenous, Injection, powder, lyophilized, for suspension - Intravenous, Injection, powder, lyophilized, for suspension, Solution - Intravenous, Solution, Powder, for suspension, Powder, for suspension - Intravenous, Liquid - Intravenous, Liquid, Injection, powder, for suspension, Injection, powder, for suspension - Intravenous, Injection, powder, for solution, Injection, powder, for solution - Intravenous

Kaposi Sarcoma

, 10.0 mg/mL, 30.0 mg/mL, 6.0 mg/mL, 100.0 mg, 5.0 mg/mL, 60.0 mg

, Intravenous, Injection, Injection - Intravenous, Injection, solution, concentrate, Injection, solution, concentrate - Intravenous, Injection, solution, Injection, solution - Intravenous, Injection, powder, lyophilized, for suspension - Intravenous, Injection, powder, lyophilized, for suspension, Solution - Intravenous, Solution, Powder, for suspension, Powder, for suspension - Intravenous, Liquid - Intravenous, Liquid, Injection, powder, for suspension, Injection, powder, for suspension - Intravenous, Injection, powder, for solution, Injection, powder, for solution - Intravenous

Neoplasm Metastasis

, 10.0 mg/mL, 30.0 mg/mL, 6.0 mg/mL, 100.0 mg, 5.0 mg/mL, 60.0 mg

, Intravenous, Injection, Injection - Intravenous, Injection, solution, concentrate, Injection, solution, concentrate - Intravenous, Injection, solution, Injection, solution - Intravenous, Injection, powder, lyophilized, for suspension - Intravenous, Injection, powder, lyophilized, for suspension, Solution - Intravenous, Solution, Powder, for suspension, Powder, for suspension - Intravenous, Liquid - Intravenous, Liquid, Injection, powder, for suspension, Injection, powder, for suspension - Intravenous, Injection, powder, for solution, Injection, powder, for solution - Intravenous

Metastatic Breast Cancer

, 10.0 mg/mL, 30.0 mg/mL, 6.0 mg/mL, 100.0 mg, 5.0 mg/mL, 60.0 mg

, Intravenous, Injection, Injection - Intravenous, Injection, solution, concentrate, Injection, solution, concentrate - Intravenous, Injection, solution, Injection, solution - Intravenous, Injection, powder, lyophilized, for suspension - Intravenous, Injection, powder, lyophilized, for suspension, Solution - Intravenous, Solution, Powder, for suspension, Powder, for suspension - Intravenous, Liquid - Intravenous, Liquid, Injection, powder, for suspension, Injection, powder, for suspension - Intravenous, Injection, powder, for solution, Injection, powder, for solution - Intravenous

Ovarian Neoplasms

, 10.0 mg/mL, 30.0 mg/mL, 6.0 mg/mL, 100.0 mg, 5.0 mg/mL, 60.0 mg

, Intravenous, Injection, Injection - Intravenous, Injection, solution, concentrate, Injection, solution, concentrate - Intravenous, Injection, solution, Injection, solution - Intravenous, Injection, powder, lyophilized, for suspension - Intravenous, Injection, powder, lyophilized, for suspension, Solution - Intravenous, Solution, Powder, for suspension, Powder, for suspension - Intravenous, Liquid - Intravenous, Liquid, Injection, powder, for suspension, Injection, powder, for suspension - Intravenous, Injection, powder, for solution, Injection, powder, for solution - Intravenous

Warnings

Abraxane Contraindications

Condition

Risk Level

Notes

neutrophil count <1500 cells/mm3

Do Not Combine

neutrophil count <1000 cells/mm3

Do Not Combine

There are 20 known major drug interactions with Abraxane.

Common Abraxane Drug Interactions

Drug Name

Risk Level

Description

2-Methoxyethanol

Major

The risk or severity of adverse effects can be increased when Paclitaxel is combined with 2-Methoxyethanol.

9-(N-methyl-L-isoleucine)-cyclosporin A

Major

The risk or severity of adverse effects can be increased when Paclitaxel is combined with 9-(N-methyl-L-isoleucine)-cyclosporin A.

Abemaciclib

Major

The metabolism of Abemaciclib can be increased when combined with Paclitaxel.

Abetimus

Major

The risk or severity of adverse effects can be increased when Paclitaxel is combined with Abetimus.

Acalabrutinib

Major

The metabolism of Acalabrutinib can be increased when combined with Paclitaxel.

Abraxane Toxicity & Overdose Risk

The lowest toxic dose of the drug in rats is 32530 micrograms per kilogram. Overdosing on this drug may lead to reduced bone marrow function, nerve damage, and inflammation of the mucous membranes. In children, overdosing may be related to alcohol poisoning.

image of a doctor in a lab doing drug, clinical research

Abraxane Novel Uses: Which Conditions Have a Clinical Trial Featuring Abraxane?

Currently, 992 active studies are being conducted to assess the potential of Abraxane to manage Ovarian Cancer, Advanced Cervical Cancer and Kaposi Sarcoma.

Condition

Clinical Trials

Trial Phases

Urinary Bladder Neoplasms

0 Actively Recruiting

Ovarian Cancer

44 Actively Recruiting

Phase 1, Phase 2, Phase 3, Early Phase 1, Not Applicable

Non-Small Cell Lung Cancer

358 Actively Recruiting

Not Applicable, Phase 2, Phase 3, Phase 1, Phase 4, Early Phase 1

Neoplasm Metastasis

26 Actively Recruiting

Phase 2, Phase 1, Phase 3, Not Applicable

advanced Thymoma

0 Actively Recruiting

Malignant Neoplasms

3 Actively Recruiting

Phase 1, Phase 2

refractory Testicular germ cell cancer

0 Actively Recruiting

Small cell carcinoma of lung

2 Actively Recruiting

Phase 1, Phase 2

Neoplasm Metastasis

0 Actively Recruiting

Head and Neck Neoplasms

0 Actively Recruiting

Ovarian Cancer

13 Actively Recruiting

Phase 1, Phase 2, Not Applicable, Phase 3

Peritoneal Neoplasms

17 Actively Recruiting

Phase 1, Phase 2, Phase 3, Not Applicable, Early Phase 1

Sarcoma

6 Actively Recruiting

Phase 1, Phase 2

Metastatic Breast Cancer

1 Actively Recruiting

Phase 1, Phase 2

Ovarian Neoplasms

9 Actively Recruiting

Phase 2, Phase 1, Not Applicable, Phase 3

Acquired Immunodeficiency Syndrome

4 Actively Recruiting

Phase 1, Phase 2, Not Applicable

Stomach Cancer

110 Actively Recruiting

Phase 2, Phase 3, Phase 1, Not Applicable, Phase 4

Kaposi Sarcoma

7 Actively Recruiting

Phase 1, Phase 2

Metastatic Melanoma

0 Actively Recruiting

Carcinoma, Non-Small-Cell Lung

13 Actively Recruiting

Phase 3, Phase 2, Early Phase 1, Not Applicable

Abraxane Reviews: What are patients saying about Abraxane?

5

Patient Review

1/3/2014

Abraxane for Breast Cancer that has Spread to Another Part of the Body

I have had great results from this treatment. My hair is thinning, but that's the only downside so far. I'm finishing my third round (3 weeks on/1 off) and the tumors in my breast have reduced to 1/4 their size, the lung lesions are reducing, and the IBC is significantly reduced and not visible.

5

Patient Review

5/31/2021

Abraxane for HR negative, HER2 negative, PD-L1 positive breast cancer

The tumor shrank so much that it could only be seen with an ultrasound. I also experienced light nausea, hair growth, and neuropathy in my fingers and around my mouth.

4.3

Patient Review

10/6/2012

Abraxane for Breast Cancer that has Spread to Another Part of the Body

I've experienced a significant reduction in my pain, ringing in my ears, and sinus problems since starting this treatment.

4

Patient Review

8/26/2013

Abraxane for Breast Cancer that has Spread to Another Part of the Body

I have experienced some nausea, extreme fatigue, and numbing in my lips and lower face. My cancer markers have gone up but I've only been on the drug for 1 month.

4

Patient Review

9/16/2015

Abraxane for Breast Cancer that has Spread to Another Part of the Body

I just completed my 10th round of treatment, and I'm feeling much better. The side effects are manageable, and the benefits have been significant according to my PET scan.

4

Patient Review

3/13/2014

Abraxane for Breast Cancer that has Spread to Another Part of the Body

I've had fifteen rounds of abraxane and found that it was very well-tolerated. The only side effect I experienced was thinning hair. However, my cancer antigen numbers have been steadily increasing, so my doctor is switching me to a different chemotherapy treatment.

4

Patient Review

1/28/2015

Abraxane for Breast Cancer that has Spread to Another Part of the Body

I received this treatment for six months, mostly in three-week intervals with one week off. I started to experience numbness and pain in my fingers and toes, which showed up on a CT scan as increased lesions in my liver. I'm now switching to eribulin.

3.7

Patient Review

9/4/2014

Abraxane for Breast Cancer that has Spread to Another Part of the Body

So far, I've had this treatment every other Friday for six weeks. The most notable side effects have been some fatigue and hair loss (though not complete baldness, thankfully). The steroids given before the IV tend to cause insomnia that night. As for how well it's working...I can't say yet. We'll need to do more scans and tests down the road to be sure.

3.3

Patient Review

5/14/2013

Abraxane for Breast Cancer that has Spread to Another Part of the Body

I was having some serious abdominal pain and this medication really helped.

3

Patient Review

5/3/2014

Abraxane for Breast Cancer that has Spread to Another Part of the Body

I'm starting this treatment and will update my review later.

3

Patient Review

11/5/2019

Abraxane for Breast Cancer that has Spread to Another Part of the Body

I just completed one session of Herceptin and Abraxane, as well as one session of Abraxane. I developed hives/rashes on my wrist, shoulder, neck and back afterwards. My dermatologist prescribed me claritin and triamcinolone, but the itching continues. Has anyone else experienced this side effect?

2.3

Patient Review

11/15/2013

Abraxane for Non-Small Cell Lung Cancer

My husband was almost able to make it through two cycles, but the side effects were so severe that he had to stop. His white blood count went perilously low and he suffered from fatigue, hair loss, aches in his legs and feet, nausea, and stomach cramps. I thought this would be a good treatment for him, but I was wrong. He'll be getting a scan next week.

1.7

Patient Review

8/10/2014

Abraxane for Breast Cancer that has Spread to Another Part of the Body

My mom is on her second round of this treatment, and she's still experiencing a lot of bone pain. She wasn't given a steroid the first time because she developed mouth sores and skin sores, so we're hoping this will be more effective.
image of drug pills surrounding a glass of water symbolizing drug consumption

Patient Q&A Section about abraxane

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

What is the difference between Taxol and Abraxane?

"Abraxane is a different form of paclitaxel than Taxol, they are both taxanes however Taxol uses a solvent called Cremophor EL to dissolve its main ingredients so the medicine can enter the bloodstream."

Answered by AI

What does Abraxane do to cancer?

"ABRAXANE works by inhibiting the function of microtubules, which are proteins that help cells divide. It is a systemic treatment, which means it is used to treat cancer that has spread to other parts of the body."

Answered by AI

What is Abraxane used for?

"metastatic melanoma

Nab-paclitaxel is a chemotherapy drug that is also known by its brand name, Abraxane. It combines the chemotherapy drug paclitaxel with a protein called albumin. It is a treatment for breast cancer that has spread and metastatic melanoma."

Answered by AI

Do you lose your hair with Abraxane?

"Some of the more common side effects that have been reported with ABRAXANE include hair loss, numbness and tingling in the extremities, and pain or weakness in the hands or feet."

Answered by AI

Clinical Trials for Abraxane

Image of Hoag Memorial Hospital Presbyterian in Newport Beach, United States.

DZ-002 for Pancreatic Cancer

18+
All Sexes
Newport Beach, CA

The goal of this clinical trial is to learn if drug DZ-002 works to treat adults with metastatic pancreatic adenocarcinoma. It will also learn about the safety of drug DZ-002. The main questions it aims to answer are: * To determine the appropriate dose of DZ-002; and * To assess the safety and efficacy of DZ-002. Participants will receive one of three different doses of the study drug through an IV over a 4-hour period on Days 1, 8, 15, and 22 of a 4-week period, or cycle. During the study, participants will have regular visits to the study clinic and multiple tests for safety and research purposes, including blood tests, along with other tests and scans. Participants will receive the study drug weekly in 4-week (28-day cycles) until there are side effects that cannot be tolerated, there is disease-worsening, or the researchers decide to stop. A post-treatment visit and a 30-day post-treatment follow up visit will be conducted after the last dose of study drug. Risks of DZ-002 include nausea, vomiting, diarrhea, chills, low levels of red blood cells, low levels of platelets, fatigue, skin rash, low blood pressure, and feeling unwell.

Phase 2
Waitlist Available

Hoag Memorial Hospital Presbyterian

Carlos Becerra, MD

Da Zen Theranostics Inc

Image of New Jersey Community Research Initiative in Newark, United States.

AI-DBT for Suicide Prevention in HIV/AIDS

18+
All Sexes
Newark, NJ

One in four older persons living with HIV/AIDS (PLWHA) report at least one suicide attempt in their lifetime, and the risk for death by suicide is 100 times higher in PLWHA than in the general population. Currently, there are no behavioral interventions that specifically address suicide prevention for older PLWHA, despite their unique biopsychosocial and structural risk factors. Through this work, investigators will adapt Dialectical Behavior Therapy, an evidence-based intervention for suicide prevention, for patients with PLWHA to be delivered by an AI-powered conversational Agent developed by our industry partner, Empower Health. Investigators will then pilot test the feasibility, usability, acceptability and preliminary efficacy to improve self-efficacy to manage negative emotions in n=50 older adults living with HIV/AIDS.

Recruiting
Has No Placebo

New Jersey Community Research Initiative (+1 Sites)

Elissa Kozlov, PhD

Have you considered Abraxane clinical trials?

We made a collection of clinical trials featuring Abraxane, we think they might fit your search criteria.
Go to Trials
Image of NEXT Dallas in Dallas, United States.

JMT108 for Cancer

18+
All Sexes
Dallas, TX

The goal of this clinical trial is to test JMT108, a type of drug called a bispecific antibody in adult patients with locally advanced or metastatic solid tumors. The main questions it aims to answer are: * To assess the safety and tolerability of JMT108 at increasing doses and determine the dose and schedule to be used in the second part of the study (Phase 1a) * To assess effectiveness of JMT108 in participants with locally advanced or metastatic tumors (Phase 1b) * To evaluate how quickly JMT108 is metabolized by the body (pharmacokinetics or PK) * To evaluate if antibodies to the study drug develop (immunogenicity) * To evaluate preliminary efficacy to the drug * To explore the pharmacodynamic (PD) characteristics of JMT108 * To explore the correlation between biomarker levels and preliminary efficacy Participants will: * Provide written informed consent * Undergo screening tests to ensure they are eligible for study treatment * Attend all required study visits and receive JMT108 by intravenous injection every 2 weeks until the study doctor determines study treatment should be stopped, based on how well a participant is doing on treatment * Be followed for progression every 3 months for up to 2 years

Phase 1
Recruiting

NEXT Dallas (+2 Sites)

Conjupro Biotherapeutics, Inc.

Image of National Institutes of Health Clinical Center in Bethesda, United States.

CYT107 for Kaposi's Sarcoma

18 - 120
All Sexes
Bethesda, MD

Background: Kaposi sarcoma (KS) is a cancer that causes abnormal tissue to grow in the skin, lymph nodes, and other organs. KS is caused by a virus known as Kaposi sarcoma herpesvirus. People infected with human immunodeficiency virus (HIV) account for 80% of KS cases in the United States. Having HIV can weaken the immune system and this can lead to KS. Weaker immune systems may be measured by low T cells (a type of immune cell). CYT107 is a human protein, made in a laboratory, that may help boost immunity, specifically by increasing T cells, in people with HIV-associated KS. Objective: To see if CYT107 can shrink KS tumors. Eligibility: People aged 18 years and older with HIV-associated KS. Design: Participants will be screened. They will have a physical exam with blood tests. Their skin lesions will be measured. They will have an x-ray of their lungs. Their ability to perform everyday tasks will be reviewed. A sample of lesion tissue (biopsy) may be collected from the skin. CYT107 is injected into the muscle of the arm, buttocks, or lower thigh once a week for up to 4 weeks. Participants will receive the shots at the clinic. Blood and other tests will be repeated at each visit. KS lesions will be measured and photographed on the 1st and 4th visits. Participants who improved after the first 4 weeks may have another 4-week treatment within a year. Follow-up visits will continue for 3 years.

Phase 2
Waitlist Available

National Institutes of Health Clinical Center

Ramya M Ramaswami, M.D.

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BI 3820768 for Ovarian Cancer

18+
All Sexes
Los Angeles, CA

This study is open to adults with advanced germ cell tumours, endometrial cancer, or ovarian cancer whose previous treatments were not successful. People can join the study if they have no remaining treatment options or if standard therapy is not suitable. The purpose of this study is to test increasing doses of BI 3820768 to find a dose that people with these types of cancer can tolerate and that may make tumours shrink. BI 3820768 is a type of treatment that may help the immune system fight cancer. This is the first time BI 3820768 is being tested in humans. The study has 2 parts based on the way BI 3820768 is given. Depending on when participants join the study, they will receive BI 3820768 through one of two ways to inject the study medicine. All participants receive the study medicine. The medicine is given as an injection once a week for 2 cycles of 3 weeks each, followed by doses every 3 weeks. Participants are in the study for up to 3 years if they are benefiting from the treatment. During this time, they visit the study site regularly, and some visits will require overnight stays. Doctors will regularly check the size of the tumour and whether it has spread. Researchers want to find the highest dose of BI 3820768 that participants can tolerate by looking at the number of participants with certain severe health problems. The doctors also regularly check participants' health, take blood samples, and note any unwanted effects.

Phase 1
Waitlist Available

Valkyrie Clinical Trials (+2 Sites)

Boehringer Ingelheim

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Virtual Exercise for Cancer

18+
All Sexes
Fort Collins, CO

The goal of this research study is to look at how live, online group exercise compares to recorded videos for helping increase physical activity levels, improve physical fitness and quality of life, and reduce loneliness among those living with and beyond cancer. The following aims have been established for this study: * Aim 1: Examine the effect of a group-based videoconference physical activity (PA) intervention on moderate to vigorous physical activity \[MVPA\] (i.e., aerobic and resistance exercise). * Aim 2: Examine the effect of the intervention on additional health-related outcomes including physical fitness (i.e., aerobic endurance, muscular strength), and quality of life at both timepoints. * Aim 3: Explore potential mediators and moderators of intervention effects. We will examine mediators (e.g., self-efficacy, outcome expectations, group cohesion) and moderators (e.g., age, cancer stage, neighborhood walkability) of the intervention on MVPA. * Exploratory Aim: Determine whether a group-based videoconference PA intervention reduces loneliness among cancer survivors. Researchers will randomize participants into one of two guided exercise groups that are 12-weeks long in duration. Participants will be asked to complete online fitness assessments and surveys as well as wear a physical activity monitor device and watch a few times throughout the study. The whole study is 9-months long in duration with a 6-month free-living period where no study activities will take place.

Recruiting
Has No Placebo

Human Performance Clinical Research Lab

Heather J Leach, PhD

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Immunotherapy Biomarkers for Non-Small Cell Lung Cancer

18+
All Sexes
Goodyear, AZ

This phase II trial tests the impact of biomarkers in predicting initial treatment (first-line) PD1 or PD-L1 (PD\[L\]-1)-based immunotherapy response and in selecting second-line treatment in patients with stage IIIB-IV non-small cell lung cancer (NSCLC). Response and survival rates in advanced stage NSCLC, unlike other cancers, rely on response to first-line therapy. Immunotherapy with PD(L)1-based therapy, may induce changes in body's immune system and may interfere with the ability of tumor cells to grow and spread. While immunotherapy has improved survival rate, the prognosis remains poor with most patients receiving chemotherapy after immunotherapy. Many types of tumors tend to lose cells or release different types of cellular products including their deoxyribonucleic acid (DNA) which is referred to as circulating tumor DNA (ctDNA) into the bloodstream before changes can be seen on scans. Health care providers can measure the level of ctDNA in blood or other bodily fluids to determine which patients are at higher risk for disease progression or relapse. The first part of this trial, studying samples of blood and tissue in the laboratory from patients receiving immunotherapy may help doctors learn more about the effects PD(L)1-based therapy on cells. It may also help doctors understand how well patients respond to treatment and may help develop new individualized treatment strategies. The second part of this trial also tests the effect of second-line immunotherapy, such as tremelimumab and durvalumab or adagrasib and bevacizumab, in treating patients with NSCLC with specific genetic mutations that is growing, spreading or getting worse (progressive). Tremelimumab is a monoclonal antibody that may interfere with the ability of tumor cells to grow and spread. A monoclonal antibody is a type of protein that can bind to certain targets in the body, such as molecules that cause the body to make an immune response (antigens). Immunotherapy with monoclonal antibodies, such as durvalumab, may help the body's immune system attack the tumor, and may interfere with the ability of tumor cells to grow and spread. Adagrasib, a type of targeted therapy, may stop the growth of tumor cells by blocking a protein needed for tumor cell growth and may kill them. Bevacizumab is in a class of medications called antiangiogenic agents. It works by stopping the formation of blood vessels that bring oxygen and nutrients to tumor. This may slow the growth and spread of tumor. Giving second-line immunotherapy, tremelimumab and durvalumab or adagrasib with bevacizumab, may be safe, tolerable, and/or effective in treating patients with stage IIIB/IV NSCLC with specific genetic mutations.

Phase 2
Waitlist Available

CTCA at Western Regional Medical Center (+12 Sites)

Ravi Salgia

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Trauma-Focused CALM for Ovarian Cancer

18+
Female
Toronto, Canada

The goal of this clinical trial is to investigate if CALM-TF (Trauma-Focused Managing Cancer and Living Meaningfully) is effective in treating traumatic stress symptoms in women with advanced ovarian cancer. It will also learn whether the efficacy differs at new diagnosis versus at recurrence. The main questions it aims to answer are: 1. What is the effectiveness of CALM-TF in reducing traumatic stress symptoms in patients with newly diagnosed or recurrent advanced ovarian cancer, as measured at 3 and 6 months? 2. What are the effects of CALM-TF on depression, quality of life, and patient-perceived benefit of the intervention compared to usual care alone? 3. What are patient perceptions of their care experiences as explored through qualitative interviews? Researchers will compare CALM-TF to usual standard of care (which includes regular conversations with medical teams and meetings with social workers) to see if CALM-TF works to treat traumatic stress. Participants will: * Receive 3-6 sessions of CALM-TF over 3-6 months (45-60 minutes each) via video call, telephone, or in-person based on preference, OR receive usual care only * Complete questionnaires at baseline, 3 months, and 6 months * Continue to receive their standard cancer care throughout the study * Some participants may be invited to participate in qualitative interviews at 6 months

Phase 3
Waitlist Available

Princess Margaret Cancer Centre

Gary Rodin, MD

Image of Memorial Sloan Kettering Cancer Center David H, Koch Center lor Cancer Care in New York, United States.

ANS014004 + EGFR-TKI for Non-Small Cell Lung Cancer

18+
All Sexes
New York, NY

Protocol Title A Study to Evaluate ANS014004 in Combination with EGFR-TKI in Patients with EGFR Mutation-Positive Locally Advanced or Metastatic Non-Small Cell Lung Cancer The main purpose of this research study is to Find a safe and tolerable dose of two investigational drugs, ANS014004 and PLB1004, when used together. Learn how effective this drug combination is at treating a type of lung cancer called "EGFR mutation-positive non-small cell lung cancer (NSCLC)" that has spread to other parts of the body (locally advanced or metastatic). This study is trying to answer the following questions: Safety \& Dosing: What are the side effects of combining ANS014004 and PLB1004? What is the best dose to use that patients can tolerate well? Effectiveness: Can this combination of drugs help shrink patients' tumors or stop them from growing? Background Information For patients with advanced lung cancer that has a specific gene change called an "EGFR mutation," targeted therapies known as EGFR-TKIs are a standard treatment. While these treatments often work well at first, most tumors eventually stop responding to the drug (this is called "acquired resistance"). The investigational drug ANS014004 is designed to block a protein called MET, which is one of the ways that tumors become resistant to EGFR-TKIs. The researchers believe that by combining ANS014004 with the EGFR-TKI PLB1004, they may be able to prevent or delay resistance, offering patients a more effective and longer-lasting treatment option. How will the study be conducted? This study is divided into two parts: Part 1 (Dose Escalation and Optimization): A small number of participants will receive different dose levels of ANS014004 combined with a fixed dose of PLB1004. The goal is to find the safest and most tolerable dose combination. Part 2 (Phase II Study): Once a recommended dose is identified, more participants will be enrolled to further evaluate how well the drug combination works against the cancer. Throughout the study, participants' health will be closely monitored, and their tumors will be measured regularly using imaging scans (like CT scans) to see how they respond to the treatment.

Phase 1 & 2
Waitlist Available

Memorial Sloan Kettering Cancer Center David H, Koch Center lor Cancer Care

Beijing Pearl Biotechnology Limited Liability Company

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