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LadRx Corp LADX

LadRx Corp is a biopharmaceutical research and development company specializing in oncology. The Company focuses on the discovery, research and clinical development of anti-cancer drug candidates that employ technologies that target chemotherapeutic drugs to solid tumors and reduce off-target toxicities. The Company’s linker activated drug release (LADR) technology platform consists of an organic backbone that is attached to a chemo toxic agent. The LADR backbone is to first target and deliver the chemo toxic agent to the tumor environment, and then to release the chemo toxic agent within the tumor. The LADR Technology offers the opportunity for multiple pipeline drugs. The LADR development efforts are focused on two classes of ultra-high potency albumin-binding drugs. These LADR-based drugs, LADRs 7, 8, 9, and 10, combine the proprietary LADR backbone with derivatives of the auristatin and maytansinoid drug classes.


OTCQB:LADX - Post by User

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Post by MissionIRon Nov 20, 2013 8:55pm
161 Views
Post# 21925366

CytRx Corp. (CYTR) Demonstrating Aldoxorubicin’s Potential a

CytRx Corp. (CYTR) Demonstrating Aldoxorubicin’s Potential a

CytRx Corp. (CYTR) Demonstrating Aldoxorubicin’s Potential as Viable Cancer Treatment, Says Trading Coach

CytRx, a biopharm research and development company specializing in oncology, was recently covered in an article by SeekingAlpha contributor John Mylant who discusses recent data that demonstrates the potential of CytRx’ aldoxorubicin as a substitute for commonly used doxorubicin. Mylant is the founder and CEO for OptionsWeekly.org and a long-time trading coach.

To read the entire article visit https://seekingalpha.com/article/1848951

Aldoxorubicin is an improved formulation of doxorubicin, a widely used chemotherapy drug. CytRx recently released interim clinical data from a phase 2b trial in which aldoxorubicin was compared to doxorubicin for the first-line treatment of soft tissue sarcomas (STS).

To summarize, results show that patients administered aldoxorubicin were able to tolerate 3.5 times the standard dose of doxorubicin with fewer side effects, resulting in greater positive response to treatment.

“The recent results from the phase 2b trial reinforces the possibility that aldoxorubicin could one day replace doxorubicin,” writes Mylant.

He also notes that at the end of September, CytRx was debt-free with approximately $23 million in short-term investments and cash equivalents.

“As with most companies in the biotech field, when the company is in research and has not yet brought a “product to the market,” it relies on raising investment capital continue to operate. I am encouraged by the interim clinical trial results to date and am optimistic for the additional phase 2b trial data which the company expects to report in December. As the company gets closer to FDA approval of aldoxorubicin, I would expect to see the share price increase in value as most biotech companies do,” said Mylant in conclusion.

For more information, visit www.cytrx.com

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