- 68% of evaluable patients with actively progressing end-stage pancreatic cancer receiving monotherapy SM-88 remain alive with a median follow-up of 4.3 months (median 5.8 months from completing last therapy)
- Of 14 patients receiving SM-88 as third-line therapy, 79% remain alive after a median follow-up of 4.7 months; survival was more than double when compared to the median expected survival of third-line pancreatic patients based on historical trials
- Median reduction of 73% in circulating tumor cell burden was reported in evaluable patients
- Study supported SM-88’s existing favorable safety profile and was well tolerated as an oral monotherapy
- TYME plans to advance SM-88 third-line pancreatic cancer registrational regulatory strategy in 2019 based on study results
- SM-88 presentation scheduled for Friday, January 18th at American Society of Clinical Oncology’s (ASCO) 2019 Gastrointestinal Cancers Symposium
NEW YORK, NY, USA I January 18, 2019 I Tyme Technologies, Inc. (NASDAQ: TYME), an emerging biotechnology company developing metabolic-based cancer therapies announces that an open label phase II clinical trial evaluating SM-88 as a monotherapy in end-stage patients with advanced pancreatic cancer demonstrated substantially improved survival benefit compared to expected median overall survival outcomes.
The 88-Panc open label phase II trial investigation involved 38 heavily pretreated patients with actively progressing metastatic pancreatic cancer who had received a median of two prior systemic therapies, and had significant disease related mortality. Researchers found that 68% of patients treated with SM-88, (19 of 28) remained alive after a median of 4.3 months of follow-up (median 5.8 months since completing prior treatment). Median survival has not been concluded for either evaluable or intent-to-treat (ITT) subjects with 60% of ITT subjects still alive.
The survival data with SM-88 is significantly longer than published results in historical trials for comparable patients. SM-88 also demonstrated anti-tumor activity by computed topography (CT), positron emission topography (PET), and circulating tumor cell burden:
- 42% (8/17) stable disease or better at two-months under RECIST criteria, including 12% (2/17) with target lesion reductions of greater than 30%
- 64% (7/11) stable disease or better at two-months using PET imaging, including reductions of up to 70%
- 74% (16/23) with circulating tumor cell reductions of 30% or greater
“We have no real options for treating end-of-life patients with advanced pancreatic cancer,” said Dr. Vincent Picozzi, Director of the Pancreaticobiliary Program at the Floyd & Delores Jones Cancer Institute at Virginia Mason Medical Center, Principal Investigator in the Tyme Phase II metastatic pancreatic cancer trial, and a Precision Promise Committee Chair. “The current survival when considering the safety of SM-88, offers new hope to both patients and physicians seeking viable treatment options for advanced patients.”
SM-88 was well tolerated with only 2 (6.5%) serious adverse events (SAEs) deemed at least potentially-related to SM-88. These SAEs both occurred in one patient, who continued on SM-88 treatment.
The 88-Panc results are from an investigational study. SM-88 is not approved for the treatment of patients with advanced pancreatic cancer.
Further details of this study will be highlighted by Dr. Vincent Picozzi and other 88-Panc primary investigators at the ASCO 2019 Gastrointestinal Cancers Symposium in San Francisco, CA on Friday, January 18, 2019, 11:30AM-1:00 PM (PST) and 5:30- 6:30 PM (PST) during the Poster Session B: “Cancers of the Pancreas, Small Bowel, and Hepatobiliary Tract” at the Moscone West Building, San Francisco. The posters will also be available on our website (www.tymeinc.com/data-publications).
Tyme management will be hosting a conference call for analysts and investors today, January 18th at 9:00AM EST to discuss the SM-88 data being presented at the ASCO GI conference. Those interested in participating in the call should dial: (877) 705-6011 (Domestic) / (201) 493-6730 (International); and enter passcode: 13686312. The call will also be viewable via webcast, which can be accessed through the “Investors” tab of the company’s website (ir.tymeinc.com). A replay of this conference call will also be available via webcast shortly after the event.
The SM-88 Posters to be presented at ASCO GI include:
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| Title: |
Phase II trial of SM-88 in Patients with Metastatic Pancreatic Cancer: Preliminary Results of the 1st Stage. (link to poster) |
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| Authors: |
Marcus Smith Noel, Andrea Wang-Gillam, Allyson J. Ocean, Sant P. Chawla, Giuseppe Del Priore, Vincent J. Picozzi |
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| Title: |
Designing Clinical Trials in 3L+ Pancreatic Cancer. (link to poster) |
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| Authors: |
Victoria G. Manax, Valery Chatikhine, Saundra Kirven, Ben R Taylor |
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| Title: |
Feasibility of SM-88 in PC After Multiple Prior Lines and ECOG <2 (NCT03512756 (link to poster) |
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| Authors: |
Marcus Smith Noel, Andrea Wang-Gillam, Allyson J. Ocean, Giuseppe Del Priore, Vincent J. Picozzi |
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| Title: |
Phase II pharmacokinetics of Oral SM-88 in Heavily Pre-Treated Advanced Pancreatic Ductal Adenocarcinoma (PC). (link to poster) |
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| Authors: |
Marcus Smith Noel, Martin Fernandez-Zapico, Gerald H. Sokol, Giuseppe Del Priore |
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About the SM-88 Study
In the SM-88 trial, a TYME-sponsored, open-label, multi-site, randomized, study of 38 advanced pancreatic cancer patients with disease progression were eligible. The primary endpoint of the study is response rate by Blinded Independent Central Review. Other endpoints including progression-free survival, overall response rate and overall survival determined by investigator, circulating tumor cell responses, and overall response rate determined by independent radiological review, as well as safety and tolerability in this end-stage patient population.
About Advanced Pancreatic Cancer
Advanced pancreatic cancer is a difficult-to-treat cancer with the lowest survival rates among all cancer types. Across all patients with pancreatic cancer, relative 5-year survival is 6% and is less than 2% for those with advanced disease. The median survival for patients in end-stage of the disease is approximately 2 months. There are two main types of pancreatic cancer – adenocarcinomas, which accounts for approximately 90% of all pancreatic cancer, and neuroendocrine tumors. Pancreatic cancer is relatively uncommon with new cases accounting for only 2.1% of all newly diagnosed cancers. However, pancreatic cancer is the fourth most common cause of cancer death for men and women in the United States.
About SM-88
SM-88 is a novel combination therapy that utilizes a proprietary dysfunctional tyrosine derivative to interrupt the metabolic processes of cancer cells, breaking down the cells’ key defenses and making them vulnerable to oxidative stress and death. SM-88 has demonstrated efficacy in the treatment of multiple oncology indications, including breast and prostate, and pancreatic cancer, without low reported toxicities or serious adverse events.
About Tyme Technologies
Tyme Technologies, Inc., is a clinical-stage biotechnology company developing cancer therapeutics that are intended to be broadly effective across tumor types and have low toxicity profiles. Unlike targeted therapies that attempt to regulate specific mutations within cancer, the Company’s therapeutic approach is designed to take advantage of a cancer cell’s innate metabolic weaknesses to compromise its defenses, leading to cell death through oxidative stress. Tyme’s lead program, SM-88, is expected to enter a pivotal trial in metastatic pancreatic cancer during 2019. For more information, visit www.tymeinc.com. Follow us on social media: @tyme
SOURCE: Tyme Technologies
Post Views: 38
- 68% of evaluable patients with actively progressing end-stage pancreatic cancer receiving monotherapy SM-88 remain alive with a median follow-up of 4.3 months (median 5.8 months from completing last therapy)
- Of 14 patients receiving SM-88 as third-line therapy, 79% remain alive after a median follow-up of 4.7 months; survival was more than double when compared to the median expected survival of third-line pancreatic patients based on historical trials
- Median reduction of 73% in circulating tumor cell burden was reported in evaluable patients
- Study supported SM-88’s existing favorable safety profile and was well tolerated as an oral monotherapy
- TYME plans to advance SM-88 third-line pancreatic cancer registrational regulatory strategy in 2019 based on study results
- SM-88 presentation scheduled for Friday, January 18th at American Society of Clinical Oncology’s (ASCO) 2019 Gastrointestinal Cancers Symposium
NEW YORK, NY, USA I January 18, 2019 I Tyme Technologies, Inc. (NASDAQ: TYME), an emerging biotechnology company developing metabolic-based cancer therapies announces that an open label phase II clinical trial evaluating SM-88 as a monotherapy in end-stage patients with advanced pancreatic cancer demonstrated substantially improved survival benefit compared to expected median overall survival outcomes.
The 88-Panc open label phase II trial investigation involved 38 heavily pretreated patients with actively progressing metastatic pancreatic cancer who had received a median of two prior systemic therapies, and had significant disease related mortality. Researchers found that 68% of patients treated with SM-88, (19 of 28) remained alive after a median of 4.3 months of follow-up (median 5.8 months since completing prior treatment). Median survival has not been concluded for either evaluable or intent-to-treat (ITT) subjects with 60% of ITT subjects still alive.
The survival data with SM-88 is significantly longer than published results in historical trials for comparable patients. SM-88 also demonstrated anti-tumor activity by computed topography (CT), positron emission topography (PET), and circulating tumor cell burden:
- 42% (8/17) stable disease or better at two-months under RECIST criteria, including 12% (2/17) with target lesion reductions of greater than 30%
- 64% (7/11) stable disease or better at two-months using PET imaging, including reductions of up to 70%
- 74% (16/23) with circulating tumor cell reductions of 30% or greater
“We have no real options for treating end-of-life patients with advanced pancreatic cancer,” said Dr. Vincent Picozzi, Director of the Pancreaticobiliary Program at the Floyd & Delores Jones Cancer Institute at Virginia Mason Medical Center, Principal Investigator in the Tyme Phase II metastatic pancreatic cancer trial, and a Precision Promise Committee Chair. “The current survival when considering the safety of SM-88, offers new hope to both patients and physicians seeking viable treatment options for advanced patients.”
SM-88 was well tolerated with only 2 (6.5%) serious adverse events (SAEs) deemed at least potentially-related to SM-88. These SAEs both occurred in one patient, who continued on SM-88 treatment.
The 88-Panc results are from an investigational study. SM-88 is not approved for the treatment of patients with advanced pancreatic cancer.
Further details of this study will be highlighted by Dr. Vincent Picozzi and other 88-Panc primary investigators at the ASCO 2019 Gastrointestinal Cancers Symposium in San Francisco, CA on Friday, January 18, 2019, 11:30AM-1:00 PM (PST) and 5:30- 6:30 PM (PST) during the Poster Session B: “Cancers of the Pancreas, Small Bowel, and Hepatobiliary Tract” at the Moscone West Building, San Francisco. The posters will also be available on our website (www.tymeinc.com/data-publications).
Tyme management will be hosting a conference call for analysts and investors today, January 18th at 9:00AM EST to discuss the SM-88 data being presented at the ASCO GI conference. Those interested in participating in the call should dial: (877) 705-6011 (Domestic) / (201) 493-6730 (International); and enter passcode: 13686312. The call will also be viewable via webcast, which can be accessed through the “Investors” tab of the company’s website (ir.tymeinc.com). A replay of this conference call will also be available via webcast shortly after the event.
The SM-88 Posters to be presented at ASCO GI include:
| |
|
|
|
|
|
| Title: |
Phase II trial of SM-88 in Patients with Metastatic Pancreatic Cancer: Preliminary Results of the 1st Stage. (link to poster) |
|
|
|
|
| Authors: |
Marcus Smith Noel, Andrea Wang-Gillam, Allyson J. Ocean, Sant P. Chawla, Giuseppe Del Priore, Vincent J. Picozzi |
|
|
|
|
| |
|
|
|
|
|
| Title: |
Designing Clinical Trials in 3L+ Pancreatic Cancer. (link to poster) |
|
|
|
|
| Authors: |
Victoria G. Manax, Valery Chatikhine, Saundra Kirven, Ben R Taylor |
|
|
|
|
| |
|
|
|
|
|
| Title: |
Feasibility of SM-88 in PC After Multiple Prior Lines and ECOG <2 (NCT03512756 (link to poster) |
|
|
|
|
| Authors: |
Marcus Smith Noel, Andrea Wang-Gillam, Allyson J. Ocean, Giuseppe Del Priore, Vincent J. Picozzi |
|
|
|
|
| |
|
|
|
|
|
| Title: |
Phase II pharmacokinetics of Oral SM-88 in Heavily Pre-Treated Advanced Pancreatic Ductal Adenocarcinoma (PC). (link to poster) |
|
|
|
|
| Authors: |
Marcus Smith Noel, Martin Fernandez-Zapico, Gerald H. Sokol, Giuseppe Del Priore |
|
|
|
|
| |
|
|
|
|
|
About the SM-88 Study
In the SM-88 trial, a TYME-sponsored, open-label, multi-site, randomized, study of 38 advanced pancreatic cancer patients with disease progression were eligible. The primary endpoint of the study is response rate by Blinded Independent Central Review. Other endpoints including progression-free survival, overall response rate and overall survival determined by investigator, circulating tumor cell responses, and overall response rate determined by independent radiological review, as well as safety and tolerability in this end-stage patient population.
About Advanced Pancreatic Cancer
Advanced pancreatic cancer is a difficult-to-treat cancer with the lowest survival rates among all cancer types. Across all patients with pancreatic cancer, relative 5-year survival is 6% and is less than 2% for those with advanced disease. The median survival for patients in end-stage of the disease is approximately 2 months. There are two main types of pancreatic cancer – adenocarcinomas, which accounts for approximately 90% of all pancreatic cancer, and neuroendocrine tumors. Pancreatic cancer is relatively uncommon with new cases accounting for only 2.1% of all newly diagnosed cancers. However, pancreatic cancer is the fourth most common cause of cancer death for men and women in the United States.
About SM-88
SM-88 is a novel combination therapy that utilizes a proprietary dysfunctional tyrosine derivative to interrupt the metabolic processes of cancer cells, breaking down the cells’ key defenses and making them vulnerable to oxidative stress and death. SM-88 has demonstrated efficacy in the treatment of multiple oncology indications, including breast and prostate, and pancreatic cancer, without low reported toxicities or serious adverse events.
About Tyme Technologies
Tyme Technologies, Inc., is a clinical-stage biotechnology company developing cancer therapeutics that are intended to be broadly effective across tumor types and have low toxicity profiles. Unlike targeted therapies that attempt to regulate specific mutations within cancer, the Company’s therapeutic approach is designed to take advantage of a cancer cell’s innate metabolic weaknesses to compromise its defenses, leading to cell death through oxidative stress. Tyme’s lead program, SM-88, is expected to enter a pivotal trial in metastatic pancreatic cancer during 2019. For more information, visit www.tymeinc.com. Follow us on social media: @tyme
SOURCE: Tyme Technologies
Post Views: 38
