Taxotere

Advance Directives, Advance Directives, Metastatic Hormone-Refractory Prostate Cancer + 13 more

Treatment

20 FDA approvals

20 Active Studies for Taxotere

What is Taxotere

Docetaxel

The Generic name of this drug

Treatment Summary

Docetaxel is an anti-cancer drug used to treat breast, ovarian, and non-small cell lung cancer. The medication works by binding to a protein found in cells called tubulin, which stops the growth of cancer cells.

Taxotere

is the brand name

image of different drug pills on a surface

Taxotere Overview & Background

Brand Name

Generic Name

First FDA Approval

How many FDA approvals?

Taxotere

Docetaxel

2008

97

Approved as Treatment by the FDA

Docetaxel, also known as Taxotere, is approved by the FDA for 20 uses such as locally advanced untreated non small cell lung cancer and Carcinoma, Non-Small-Cell Lung .

locally advanced untreated non small cell lung cancer

Used to treat locally advanced untreated non small cell lung cancer in combination with Cisplatin

Carcinoma, Non-Small-Cell Lung

Used to treat metastatic untreated non small cell lung cancer in combination with Cisplatin

Neoplasm Metastasis

Metastatic Hormone-Refractory Prostate Cancer

Used to treat refractory, metastatic hormone-refractory Prostate cancer in combination with Prednisone

Node Positive Breast Cancer

Used to treat Node Positive Breast Cancer in combination with Cyclophosphamide

Advance Directives

Used to treat advanced untreated gastric adenocarcinoma in combination with Cisplatin

metastatic untreated non small cell lung cancer

Used to treat metastatic untreated non small cell lung cancer in combination with Cisplatin

Non-Small Cell Lung Carcinoma

Metastatic Breast Cancer

Advance Directives

Ovarian Cancer Metastatic

refractory, metastatic Non small cell lung cancer

refractory, metastatic hormone-refractory Prostate cancer

Used to treat refractory, metastatic hormone-refractory Prostate cancer in combination with Prednisone

Metastatic Squamous Cell Carcinoma of the Head and Neck (HNSCC)

Metastatic Breast Cancer

Squamous Cell Carcinoma of Head and Neck

BRCA1 gene

Malignant Neoplasms

Used to treat Node Positive Breast Cancer in combination with Cyclophosphamide

Advance Directives

Used to treat locally advanced untreated non small cell lung cancer in combination with Cisplatin

Advance Directives

Used to treat locally advanced Squamous cell carcinoma of head and neck in combination with Cisplatin

Effectiveness

How Taxotere Affects Patients

Docetaxel is a drug used to treat cancer. It helps create and stabilize microtubules, which are necessary for many cell functions. Docetaxel also changes the way microtubules are organized, which can prevent cancer cells from dividing and growing.

How Taxotere works in the body

Docetaxel stops cancer cells from reproducing by blocking the growth of their microtubules. This is done by locking the "building blocks" of microtubules (tubulin) in place, preventing them from moving around. This interferes with cell function, as this movement of microtubules is important for transporting chromosomes during mitosis (cell division). Additionally, docetaxel works by binding to a protein called Bcl-2, which stops cells from undergoing programmed cell death (apoptosis). By binding to this protein, docetaxel prevents it from working and allows the cell to die.

When to interrupt dosage

The advised dosage of Taxotere is contingent upon the determined condition, for example, Esophageal Cancer, Neoplasm Metastasis and Non-Small Cell Lung Carcinoma. The measure of dosage deviates, in accordance with the approach of administration (e.g. Intravenous or Injection, solution, concentrate - Intravenous) presented in the following table.

Condition

Dosage

Administration

Metastatic Hormone-Refractory Prostate Cancer

20.0 mg/mL, 80.0 mg/mL, , 10.0 mg/mL, 80.0 mg, 20.0 mg, 160.0 mg/mL, 180.0 mg/mL, 120.0 mg/mL, 200.0 mg/mL, 140.0 mg/mL, 40.0 mg/mL, 16.0 mg/mL

Intravenous, Injection, solution, concentrate, Injection, solution, concentrate - Intravenous, , Kit, Injection, solution - Intravenous, Injection, solution, Injection - Intravenous, Injection, Solution - Intravenous, Solution, Kit; Solution, Kit; Solution - Intravenous

Malignant Neoplasms

20.0 mg/mL, 80.0 mg/mL, , 10.0 mg/mL, 80.0 mg, 20.0 mg, 160.0 mg/mL, 180.0 mg/mL, 120.0 mg/mL, 200.0 mg/mL, 140.0 mg/mL, 40.0 mg/mL, 16.0 mg/mL

Intravenous, Injection, solution, concentrate, Injection, solution, concentrate - Intravenous, , Kit, Injection, solution - Intravenous, Injection, solution, Injection - Intravenous, Injection, Solution - Intravenous, Solution, Kit; Solution, Kit; Solution - Intravenous

Small Cell Lung Cancer

20.0 mg/mL, 80.0 mg/mL, , 10.0 mg/mL, 80.0 mg, 20.0 mg, 160.0 mg/mL, 180.0 mg/mL, 120.0 mg/mL, 200.0 mg/mL, 140.0 mg/mL, 40.0 mg/mL, 16.0 mg/mL

Intravenous, Injection, solution, concentrate, Injection, solution, concentrate - Intravenous, , Kit, Injection, solution - Intravenous, Injection, solution, Injection - Intravenous, Injection, Solution - Intravenous, Solution, Kit; Solution, Kit; Solution - Intravenous

Urinary Bladder Neoplasms

20.0 mg/mL, 80.0 mg/mL, , 10.0 mg/mL, 80.0 mg, 20.0 mg, 160.0 mg/mL, 180.0 mg/mL, 120.0 mg/mL, 200.0 mg/mL, 140.0 mg/mL, 40.0 mg/mL, 16.0 mg/mL

Intravenous, Injection, solution, concentrate, Injection, solution, concentrate - Intravenous, , Kit, Injection, solution - Intravenous, Injection, solution, Injection - Intravenous, Injection, Solution - Intravenous, Solution, Kit; Solution, Kit; Solution - Intravenous

Soft Tissue Sarcoma

20.0 mg/mL, 80.0 mg/mL, , 10.0 mg/mL, 80.0 mg, 20.0 mg, 160.0 mg/mL, 180.0 mg/mL, 120.0 mg/mL, 200.0 mg/mL, 140.0 mg/mL, 40.0 mg/mL, 16.0 mg/mL

Intravenous, Injection, solution, concentrate, Injection, solution, concentrate - Intravenous, , Kit, Injection, solution - Intravenous, Injection, solution, Injection - Intravenous, Injection, Solution - Intravenous, Solution, Kit; Solution, Kit; Solution - Intravenous

Neoplasm Metastasis

20.0 mg/mL, 80.0 mg/mL, , 10.0 mg/mL, 80.0 mg, 20.0 mg, 160.0 mg/mL, 180.0 mg/mL, 120.0 mg/mL, 200.0 mg/mL, 140.0 mg/mL, 40.0 mg/mL, 16.0 mg/mL

Intravenous, Injection, solution, concentrate, Injection, solution, concentrate - Intravenous, , Kit, Injection, solution - Intravenous, Injection, solution, Injection - Intravenous, Injection, Solution - Intravenous, Solution, Kit; Solution, Kit; Solution - Intravenous

Squamous Cell Carcinoma of Head and Neck

20.0 mg/mL, 80.0 mg/mL, , 10.0 mg/mL, 80.0 mg, 20.0 mg, 160.0 mg/mL, 180.0 mg/mL, 120.0 mg/mL, 200.0 mg/mL, 140.0 mg/mL, 40.0 mg/mL, 16.0 mg/mL

Intravenous, Injection, solution, concentrate, Injection, solution, concentrate - Intravenous, , Kit, Injection, solution - Intravenous, Injection, solution, Injection - Intravenous, Injection, Solution - Intravenous, Solution, Kit; Solution, Kit; Solution - Intravenous

Advance Directives

20.0 mg/mL, 80.0 mg/mL, , 10.0 mg/mL, 80.0 mg, 20.0 mg, 160.0 mg/mL, 180.0 mg/mL, 120.0 mg/mL, 200.0 mg/mL, 140.0 mg/mL, 40.0 mg/mL, 16.0 mg/mL

Intravenous, Injection, solution, concentrate, Injection, solution, concentrate - Intravenous, , Kit, Injection, solution - Intravenous, Injection, solution, Injection - Intravenous, Injection, Solution - Intravenous, Solution, Kit; Solution, Kit; Solution - Intravenous

Advance Directives

20.0 mg/mL, 80.0 mg/mL, , 10.0 mg/mL, 80.0 mg, 20.0 mg, 160.0 mg/mL, 180.0 mg/mL, 120.0 mg/mL, 200.0 mg/mL, 140.0 mg/mL, 40.0 mg/mL, 16.0 mg/mL

Intravenous, Injection, solution, concentrate, Injection, solution, concentrate - Intravenous, , Kit, Injection, solution - Intravenous, Injection, solution, Injection - Intravenous, Injection, Solution - Intravenous, Solution, Kit; Solution, Kit; Solution - Intravenous

Advance Directives

20.0 mg/mL, 80.0 mg/mL, , 10.0 mg/mL, 80.0 mg, 20.0 mg, 160.0 mg/mL, 180.0 mg/mL, 120.0 mg/mL, 200.0 mg/mL, 140.0 mg/mL, 40.0 mg/mL, 16.0 mg/mL

Intravenous, Injection, solution, concentrate, Injection, solution, concentrate - Intravenous, , Kit, Injection, solution - Intravenous, Injection, solution, Injection - Intravenous, Injection, Solution - Intravenous, Solution, Kit; Solution, Kit; Solution - Intravenous

Non-Small Cell Lung Carcinoma

20.0 mg/mL, 80.0 mg/mL, , 10.0 mg/mL, 80.0 mg, 20.0 mg, 160.0 mg/mL, 180.0 mg/mL, 120.0 mg/mL, 200.0 mg/mL, 140.0 mg/mL, 40.0 mg/mL, 16.0 mg/mL

Intravenous, Injection, solution, concentrate, Injection, solution, concentrate - Intravenous, , Kit, Injection, solution - Intravenous, Injection, solution, Injection - Intravenous, Injection, Solution - Intravenous, Solution, Kit; Solution, Kit; Solution - Intravenous

Sarcoma

20.0 mg/mL, 80.0 mg/mL, , 10.0 mg/mL, 80.0 mg, 20.0 mg, 160.0 mg/mL, 180.0 mg/mL, 120.0 mg/mL, 200.0 mg/mL, 140.0 mg/mL, 40.0 mg/mL, 16.0 mg/mL

Intravenous, Injection, solution, concentrate, Injection, solution, concentrate - Intravenous, , Kit, Injection, solution - Intravenous, Injection, solution, Injection - Intravenous, Injection, Solution - Intravenous, Solution, Kit; Solution, Kit; Solution - Intravenous

BRCA1 gene

20.0 mg/mL, 80.0 mg/mL, , 10.0 mg/mL, 80.0 mg, 20.0 mg, 160.0 mg/mL, 180.0 mg/mL, 120.0 mg/mL, 200.0 mg/mL, 140.0 mg/mL, 40.0 mg/mL, 16.0 mg/mL

Intravenous, Injection, solution, concentrate, Injection, solution, concentrate - Intravenous, , Kit, Injection, solution - Intravenous, Injection, solution, Injection - Intravenous, Injection, Solution - Intravenous, Solution, Kit; Solution, Kit; Solution - Intravenous

Advance Directives

20.0 mg/mL, 80.0 mg/mL, , 10.0 mg/mL, 80.0 mg, 20.0 mg, 160.0 mg/mL, 180.0 mg/mL, 120.0 mg/mL, 200.0 mg/mL, 140.0 mg/mL, 40.0 mg/mL, 16.0 mg/mL

Intravenous, Injection, solution, concentrate, Injection, solution, concentrate - Intravenous, , Kit, Injection, solution - Intravenous, Injection, solution, Injection - Intravenous, Injection, Solution - Intravenous, Solution, Kit; Solution, Kit; Solution - Intravenous

Metastatic Breast Cancer

20.0 mg/mL, 80.0 mg/mL, , 10.0 mg/mL, 80.0 mg, 20.0 mg, 160.0 mg/mL, 180.0 mg/mL, 120.0 mg/mL, 200.0 mg/mL, 140.0 mg/mL, 40.0 mg/mL, 16.0 mg/mL

Intravenous, Injection, solution, concentrate, Injection, solution, concentrate - Intravenous, , Kit, Injection, solution - Intravenous, Injection, solution, Injection - Intravenous, Injection, Solution - Intravenous, Solution, Kit; Solution, Kit; Solution - Intravenous

Carcinoma, Non-Small-Cell Lung

20.0 mg/mL, 80.0 mg/mL, , 10.0 mg/mL, 80.0 mg, 20.0 mg, 160.0 mg/mL, 180.0 mg/mL, 120.0 mg/mL, 200.0 mg/mL, 140.0 mg/mL, 40.0 mg/mL, 16.0 mg/mL

Intravenous, Injection, solution, concentrate, Injection, solution, concentrate - Intravenous, , Kit, Injection, solution - Intravenous, Injection, solution, Injection - Intravenous, Injection, Solution - Intravenous, Solution, Kit; Solution, Kit; Solution - Intravenous

Warnings

Taxotere has one contraindication and should not be used when encountering the conditions contained in the following table.

Taxotere Contraindications

Condition

Risk Level

Notes

neutrophil count <1500 cells/mm3

Do Not Combine

There are 20 known major drug interactions with Taxotere.

Common Taxotere Drug Interactions

Drug Name

Risk Level

Description

2-Methoxyethanol

Major

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

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

Major

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

Abemaciclib

Major

The metabolism of Abemaciclib can be decreased when combined with Docetaxel.

Abetimus

Major

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

Acteoside

Major

The risk or severity of adverse effects can be increased when Docetaxel is combined with Acteoside.

Taxotere Toxicity & Overdose Risk

The most toxic dose of this drug in rats is greater than 2000mg/kg. An overdose could lead to problems with the bone marrow, peripheral nerve damage, and irritation of the mucous membranes. Two people who overdosed on this drug experienced severe low white blood cell counts, fatigue, skin reactions, and tingling. They both recovered without any major problems.

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

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

378 active trials are being conducted to assess the potential of Taxotere to combat metastatic untreated non small cell lung cancer, Sarcoma and Advance Directives.

Condition

Clinical Trials

Trial Phases

Metastatic Hormone-Refractory Prostate Cancer

79 Actively Recruiting

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

Metastatic Breast Cancer

1 Actively Recruiting

Phase 1, Phase 2

BRCA1 gene

12 Actively Recruiting

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

Non-Small Cell Lung Carcinoma

714 Actively Recruiting

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

Advance Directives

0 Actively Recruiting

Small Cell Lung Cancer

50 Actively Recruiting

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

Advance Directives

0 Actively Recruiting

Carcinoma, Non-Small-Cell Lung

0 Actively Recruiting

Neoplasm Metastasis

1 Actively Recruiting

Phase 2

Soft Tissue Sarcoma

51 Actively Recruiting

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

Advance Directives

0 Actively Recruiting

Squamous Cell Carcinoma of Head and Neck

6 Actively Recruiting

Phase 1, Phase 2, Phase 3

Sarcoma

1 Actively Recruiting

Phase 2

Advance Directives

0 Actively Recruiting

Malignant Neoplasms

4 Actively Recruiting

Not Applicable, Phase 2

Urinary Bladder Neoplasms

0 Actively Recruiting

Taxotere Reviews: What are patients saying about Taxotere?

4.7

Patient Review

8/8/2016

Taxotere for Breast Cancer

I was diagnosed with Triple Negative Breast Cancer and started Taxotere immediately. Almost all of my hair fell out, as well as my nails. The nail beds turned black and now, 3 months later, the nails are coming off. My hair is slowly growing back but it's a different texture. I didn't have any unexpected side effects which was great.

3.7

Patient Review

4/13/2015

Taxotere for Cancer of Prostate that has Spread to Other Part of Body

I've only had 2 out of 6 infusions. Too early to tell if its effective. Will update after next PSA test. My tolerance is very good. The only negatives were an early swelling of hands (now OK) and fatigue; both side affects have improved since then, however.

3.3

Patient Review

6/29/2011

Taxotere for Cancer of Prostate that has Spread to Other Part of Body

I've only just started taking this medication, so I don't have a ton of information yet.

3.3

Patient Review

3/3/2010

Taxotere for Breast Cancer

3.3

Patient Review

1/31/2013

Taxotere for Cancer Involving the Head or Neck

2003 is when I was treated with this drug. I had an allergic reaction in which my feet burned like I walked on hot coals. I could not walk and soon layers and layers of the skin peeled off and lost toenails and finger nails and all the skin on my hands. Ever since I have had severe nerve damage. I do not have active cancer however. They did switch me to Taxol to finish my treatments.

2.7

Patient Review

8/18/2011

Taxotere for Non-Small Cell Lung Cancer

Taxotere caused me significant and permanent damage to my lungs. If you find yourself short of breath after this treatment, please get examined by a doctor immediately.

2.7

Patient Review

3/5/2010

Taxotere for Non-Small Cell Lung Cancer

2.3

Patient Review

7/20/2011

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

I've had three infusions of this treatment. While it has been successful in reducing my PSA levels, I have also had reactions to it during the infusion process that have caused chest and neck pain.

2

Patient Review

9/11/2011

Taxotere for Breast Cancer

I constantly had diarrhea, felt nauseous, and experienced chronic pain in my muscles and joints.

2

Patient Review

3/14/2014

Taxotere for Non-Small Cell Lung Cancer

i had every side effect mentioned, great for working on cancer, horable working on you it's a killer. wound up with chf,copd,more lung trouble. took myself off the drug after 9 sessions. now trying to rehab.

1

Patient Review

7/22/2010

Taxotere for Cancer Involving the Head or Neck

I've been taking Taxotere for seven months now, and the constant eye tearing and fingernail infections are really getting to me. My CT scans have shown "slight improvement," but I'm not sure if that's worth the side effects. I'm planning on discussing a change in treatment with my oncologist at my next appointment.

1

Patient Review

6/18/2014

Taxotere for Breast Cancer

I had my 1st TCH on 6/11/14. Within 12 hours, I was in excruciating pain from lower back to knees. The pain lasted 3 days. On day 6, my infusion arm started turning red and itching. Day 7, I have a rash on my infusion hand/wrist that is red and itchy. My mouth and tongue are swollen and I have sores on the sides of my tongue. I have 5 more rounds to go. I am meeting with my Oncologist before my next treatment on 7/1/14. Praying he will change my treatment plan!
image of drug pills surrounding a glass of water symbolizing drug consumption

Patient Q&A Section about taxotere

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

What are the side effects of Taxotere?

"-Side effects such as pain or swelling at the injection site, nausea, vomiting, diarrhea, excessive tearing, fatigue, dizziness, drowsiness, feeling drunk, constipation, and loss of appetite may occur.

-Temporary hair loss and nail changes may also occur.

-This medication can decrease your body's ability to fight an infection."

Answered by AI

What is the most common side effect of docetaxel?

"Two common long-term side effects of docetaxel chemotherapy are sensory and motor peripheral neuropathy, which are less severe than with paclitaxel. Grade 3 and 4 neuropathy is only observed in less than 10% of patients receiving docetaxel therapy."

Answered by AI

How long can you take Taxotere?

"Health care providers give Taxotere to their patients through an IV. The IV takes one hour to administer the drug, and this happens every three weeks. Depending on the type of cancer, the patient may have to go through several cycles of this treatment."

Answered by AI

Is Taxotere a strong chemo drug?

"Because Taxotere is a strong chemotherapy drug, its side effects tend to be more extreme than drugs that treat other, less serious issues. To deal with these side effects, doctors may lower the dose or prescribe drugs that reduce the risk of allergic reactions."

Answered by AI

Clinical Trials for Taxotere

Image of Henry Ford Cancer- Detroit in Detroit, United States.

SG + Immunotherapy for Lung Cancer

18+
All Sexes
Detroit, MI

The goal of this clinical trial is to learn if the combination of sacituzumab govetican (SG) and atezolizumab/durvalumab is effective in controlling cancer tumor growth in adults with extensive stage small cell lung cancer. These drugs are FDA approved individually in different cancers. This combination is evaluated in breast cancer and showed promising combination. The effectiveness of this treatment combination will be measured by changes in tumor size and appearance of new tumors. Participants in the trial will: * receive treatment SG and immunotherapy every 21 days for up to 2 years or until it is no longer works for the patient. * CT scans at 6weeks for first 6 cycles and then every 9-12 weeks and MRI brain every 12 weeks. * provide tissue (optional) and blood for additional testing (learn about the cancer).

Phase 2
Waitlist Available

Henry Ford Cancer- Detroit

Gilead Sciences

Image of University of North Carolina in Chapel Hill, United States.

Pembrolizumab and Radiation for Triple Negative Breast Cancer

18+
All Sexes
Chapel Hill, NC

This is a prospective radiation dose-finding, phase 2 expansion study of the Triple Negative (TN) cohort of the multicenter randomized study P-RAD (A Randomized Study of Preoperative Chemotherapy, Pembrolizumab and No, Low or High Dose RADiation in Node-Positive, HER2-Negative Breast Cancer; NCT04443348) that seeks to establish the optimal dose of radiation therapy (RT) to elicit an immune response when combined with immune checkpoint inhibitor (ICI) in breast cancer patients. Eligible subjects include women or men with operable, lymph node-positive, triple negative (TN) breast cancer who are candidates for standard of care neoadjuvant chemo-immunotherapy (NAC) based on the KEYNOTE-522 clinical trial. Thirty-two (n=32) patients will be randomized 1:1 to receive either low RT boost (9Gy total) or high RT boost (24Gy total). All RT will be delivered to the intact breast tumor in 3 daily fractions over 3 days. In the Neoadjuvant Phase, the first cycle (C1) of pembrolizumab (200 mg i.v.) will be administered within 0-2 days of initiating RT. Participation in this study requires availability of residual diagnostic tissue biopsies of the primary tumor and metastatic lymph node for research use. If this tissue is not available, baseline research biopsies will be performed. Additionally, a research biopsy of the breast tumor and lymph node is required on Day 10-14 of C1 of pembrolizumab. After completion of the research biopsy in Week 2, the participants can commence standard-of-care neoadjuvant chemotherapy and pembrolizumab at the discretion of their medical oncology provider. After completing NAC, participants will undergo standard of care surgical resection of the breast and axillary lymph nodes, at the discretion of their surgical oncology provider. In the Adjuvant Phase, participants will receive standard of care adjuvant systemic therapy and standard of care adjuvant radiotherapy (if indicated), although recognizing that the breast tumor boost portion of this treatment has already been administered preoperatively. Except for late radiation adverse reactions of special interest, which will be followed yearly for up to 5 years, follow-up will occur every 6 months for 3 years.

Phase 2
Waitlist Available

University of North Carolina

Dana Casey, MD

Merck Sharp & Dohme LLC

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Image of The Ottawa Hospital Cancer Centre in Ottawa, Canada.

Endocrine Therapy for Breast and Prostate Cancer

18+
All Sexes
Ottawa, Canada

The REaCT-CHRONO-MetBP Pilot study will compare morning and evening administration of endocrine-based therapy in metastatic breast and prostate cancers. Participants with metastatic breast or prostate cancer will be randomly placed in one of two groups: a morning group and an evening group. The group assignment will determine whether they take their endocrine therapy in the morning or the evening. The primary outcome of this pilot study is to evaluate the feasibility of study procedures in order to conduct a larger definitive trial in the future. The secondary outcomes include comparing quality of life, tolerability, and efficacy outcomes between the morning and evening groups for each of the two cancer cohorts (metastatic breast and prostate cancer).

Phase 4
Waitlist Available

The Ottawa Hospital Cancer Centre

Marie-France Savard, MD

Image of Washington University School of Medicine in St Louis, United States.

Cirtuvivint + Irinotecan for Small Cell Lung Cancer

18+
All Sexes
St Louis, MO

Although small cell lung cancer (SCLC) responds dramatically to initial platinum-based chemotherapy, recurrences are nearly universal. The addition of atezolizumab, an immune checkpoint inhibitor, to front-line chemotherapy has recently demonstrated an improvement in overall survival (OS) in extensive stage SCLC (ES-SCLC). Subsequent lines of therapies are associated with modest efficacy in patients with relapsed disease, and the median overall survival is still 12 to 13 months at best. Cirtuvivint is a small molecule inhibitor of the CDC2-like kinases (CLKs) and dual-specificity tyrosine-regulated kinases (DYRKs); inhibiting CLKs and DYRKs has been shown in preclinical models to cause tumor growth inhibition and sensitize cancer cells to cytotoxic chemotherapy. This study is testing the hypothesis that adding cirtuvivint to chemotherapy in patients with relapsed SCLC will be well tolerated and improve the response rate and progression-free survival (PFS).

Phase 1 & 2
Recruiting

Washington University School of Medicine

Ramaswamy Govindan, M.D.

Biosplice Therapeutics, Inc.

Have you considered Taxotere clinical trials?

We made a collection of clinical trials featuring Taxotere, we think they might fit your search criteria.
Go to Trials

Have you considered Taxotere clinical trials?

We made a collection of clinical trials featuring Taxotere, we think they might fit your search criteria.
Go to Trials