Market Cap 88.32M
Revenue (ttm) 0.00
Net Income (ttm) -23.14M
EPS (ttm) N/A
PE Ratio 0.00
Forward PE N/A
Profit Margin 0.00%
Debt to Equity Ratio 0.00
Volume 561,587
Avg Vol 917,426
Day's Range N/A - N/A
Shares Out 100.36M
Stochastic %K 63%
Beta 0.88
Analysts Strong Sell
Price Target $5.01

Company Profile

Oncolytics Biotech Inc., a clinical-stage biopharmaceutical company, engages in the research, development, and commercialization of oncology treatments. The company develops pelareorep, an intravenously delivered immunotherapeutic agent for the treatment of hormone receptor-positive / human epidermal growth factor 2-negative advanced and metastatic breast cancer, metastatic pancreatic ductal adenocarcinoma, and anal cancer. It has an agreement with Roche Holding AG to supply its immune checkpoin...

Industry: Biotechnology
Sector: Healthcare
Phone: 403 670 7377
Fax: 403 283 0858
Address:
322 11th Avenue SW, Suite 804, Calgary, Canada
GoPatzGo123
GoPatzGo123 Dec. 5 at 9:49 PM
$ONCY just staying.... 👇👇👇
0 · Reply
FoxM07
FoxM07 Dec. 5 at 9:19 PM
$ONCY RVMD up $1.16 to close at $79.64...Oncy up $0.011 to remain on the wrong side of a buck. So who's winning Mr delusional?
0 · Reply
GoPatzGo123
GoPatzGo123 Dec. 5 at 9:18 PM
$ONCY dont understand these price targets anywhere from 3 to most recent $10 how many have we seen and none of them have been right over the last $5 years.
1 · Reply
Notable_Ex
Notable_Ex Dec. 5 at 8:27 PM
$ONCY Royalty Pharma' and its synthetic royalty funding in RVMD is certainly one of those 'market' players and analysts who are trying to "will" RVMD onwards. Royalty's risk in RVMD has been crystallized by virtue of the amount of Royalty Pharma's loan to RVMD. Now its been mitigating their risk through trading strategies that are purposely driving up RVMD's share price to bring in institutional and public monies, so that Royalty can recover theirs.
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Notable_Ex
Notable_Ex Dec. 5 at 8:26 PM
$ONCY Once again the market and analysts are trying to "will" RVMD and keep overlooking the proof in RVMD's clinical results and the company's decision not to move forward with a planned H225 clinical study involving daraxonrasib in first line PDAC in combination with chemotherapy, primarily on the lack of efficacy and long-term durability which would require OS as the primary endpoint. Consequently RVMD is 'caught on the horns of a dilemma' - to agree with the FDA's second line relegation in PDAC or risk everything and try to run a trial in first line PDAC, when historicla data shows that daraxonrasib would be likely to be unsuccessful due to daraxonrasib's overalapping toxicities in combination with chemotherapy and unproven efficacy, given their trials never included OS as the primary endpoint, which the FDA now requires that a drug demonstrates in order to be approved - particularly now that the FDA has moved to a single-trial approval process.
0 · Reply
FoxM07
FoxM07 Dec. 5 at 8:24 PM
$ONCY RVMD is too massive and successful to properly compare to an ignored 30 year old biotech.
0 · Reply
GoPatzGo123
GoPatzGo123 Dec. 5 at 8:12 PM
$TGL add $ONCY to your radar.
0 · Reply
Notable_Ex
Notable_Ex Dec. 5 at 7:41 PM
$ONCY RVMD's clinical results and the company's decision not to move forward with a planned H225 clinical study involving daraxonrasib in first line PDAC in combination with chemotherapy, primarily on the lack of efficacy and long-term durability which would require OS as the primary endpoint.. and the FDA's decision to move forward with single-trial data for approval, precludes RVMD moving forward. Consequently RVMD is 'caught on the horns of a dilemma' - to agree with the FDA's second line relegation in PDAC or risk everything and try to run a trial in first line PDAC, when historical data shows that daraxonrasib would be likely to be unsuccessful in first line therap due to daraxonrasib's overalapping toxicities in combination with chemotherapy and unproven efficacy, given their trials never included OS as the primary endpoint, which the FDA now requires that a drug demonstrates in order to be approved - particularly now that the FDA has moved to a single-trial approval process.
0 · Reply
FoxM07
FoxM07 Dec. 5 at 5:12 PM
$ONCY as previously stated, rampant delusional conjecture doesn't factor in when determining the acquisition value of a company. Oncy is a penny stock struggling to get attention and cash. Who knows if Pela and Jared's slightly more honed business acumen will lead to something, but here's hoping.
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Ichigodoran
Ichigodoran Dec. 5 at 4:17 PM
$ONCY The Company is advancing pelareorep in combination with chemotherapy and/or checkpoint inhibitors in metastatic pancreatic and breast cancers, of which both development programs have received Fast Track designation from the FDA, and other gastrointestinal tumors. Oncolytics is actively pursuing strategic partnerships to accelerate development and maximize commercial impact.
0 · Reply
Latest News on ONCY
Oncolytics Biotech Inc. (ONCY) Q1 2025 Earnings Call Transcript

May 14, 2025, 7:21 PM EDT - 7 months ago

Oncolytics Biotech Inc. (ONCY) Q1 2025 Earnings Call Transcript


Oncolytics Biotech Inc. (ONCY) Q4 2024 Earnings Call Transcript

Mar 7, 2025, 11:11 AM EST - 9 months ago

Oncolytics Biotech Inc. (ONCY) Q4 2024 Earnings Call Transcript


GoPatzGo123
GoPatzGo123 Dec. 5 at 9:49 PM
$ONCY just staying.... 👇👇👇
0 · Reply
FoxM07
FoxM07 Dec. 5 at 9:19 PM
$ONCY RVMD up $1.16 to close at $79.64...Oncy up $0.011 to remain on the wrong side of a buck. So who's winning Mr delusional?
0 · Reply
GoPatzGo123
GoPatzGo123 Dec. 5 at 9:18 PM
$ONCY dont understand these price targets anywhere from 3 to most recent $10 how many have we seen and none of them have been right over the last $5 years.
1 · Reply
Notable_Ex
Notable_Ex Dec. 5 at 8:27 PM
$ONCY Royalty Pharma' and its synthetic royalty funding in RVMD is certainly one of those 'market' players and analysts who are trying to "will" RVMD onwards. Royalty's risk in RVMD has been crystallized by virtue of the amount of Royalty Pharma's loan to RVMD. Now its been mitigating their risk through trading strategies that are purposely driving up RVMD's share price to bring in institutional and public monies, so that Royalty can recover theirs.
0 · Reply
Notable_Ex
Notable_Ex Dec. 5 at 8:26 PM
$ONCY Once again the market and analysts are trying to "will" RVMD and keep overlooking the proof in RVMD's clinical results and the company's decision not to move forward with a planned H225 clinical study involving daraxonrasib in first line PDAC in combination with chemotherapy, primarily on the lack of efficacy and long-term durability which would require OS as the primary endpoint. Consequently RVMD is 'caught on the horns of a dilemma' - to agree with the FDA's second line relegation in PDAC or risk everything and try to run a trial in first line PDAC, when historicla data shows that daraxonrasib would be likely to be unsuccessful due to daraxonrasib's overalapping toxicities in combination with chemotherapy and unproven efficacy, given their trials never included OS as the primary endpoint, which the FDA now requires that a drug demonstrates in order to be approved - particularly now that the FDA has moved to a single-trial approval process.
0 · Reply
FoxM07
FoxM07 Dec. 5 at 8:24 PM
$ONCY RVMD is too massive and successful to properly compare to an ignored 30 year old biotech.
0 · Reply
GoPatzGo123
GoPatzGo123 Dec. 5 at 8:12 PM
$TGL add $ONCY to your radar.
0 · Reply
Notable_Ex
Notable_Ex Dec. 5 at 7:41 PM
$ONCY RVMD's clinical results and the company's decision not to move forward with a planned H225 clinical study involving daraxonrasib in first line PDAC in combination with chemotherapy, primarily on the lack of efficacy and long-term durability which would require OS as the primary endpoint.. and the FDA's decision to move forward with single-trial data for approval, precludes RVMD moving forward. Consequently RVMD is 'caught on the horns of a dilemma' - to agree with the FDA's second line relegation in PDAC or risk everything and try to run a trial in first line PDAC, when historical data shows that daraxonrasib would be likely to be unsuccessful in first line therap due to daraxonrasib's overalapping toxicities in combination with chemotherapy and unproven efficacy, given their trials never included OS as the primary endpoint, which the FDA now requires that a drug demonstrates in order to be approved - particularly now that the FDA has moved to a single-trial approval process.
0 · Reply
FoxM07
FoxM07 Dec. 5 at 5:12 PM
$ONCY as previously stated, rampant delusional conjecture doesn't factor in when determining the acquisition value of a company. Oncy is a penny stock struggling to get attention and cash. Who knows if Pela and Jared's slightly more honed business acumen will lead to something, but here's hoping.
0 · Reply
Ichigodoran
Ichigodoran Dec. 5 at 4:17 PM
$ONCY The Company is advancing pelareorep in combination with chemotherapy and/or checkpoint inhibitors in metastatic pancreatic and breast cancers, of which both development programs have received Fast Track designation from the FDA, and other gastrointestinal tumors. Oncolytics is actively pursuing strategic partnerships to accelerate development and maximize commercial impact.
0 · Reply
Notable_Ex
Notable_Ex Dec. 5 at 4:04 PM
$ONCY As previously stated: ONCY = $15+ Billion just on RVMD comparables and Roche's /Royalty Pharma's financial support of RVMD, would have daraxonrasib a follow-on therapy to pelareorep + chemotherapy/folfirinox + ICI first line combination therapy in PDAC, for example
0 · Reply
Notable_Ex
Notable_Ex Dec. 5 at 4:01 PM
$ONCY Of note: Roche, Royalty Pharma, and Revolution Medicines (RVMD) are linked through a 2025 strategic funding arrangement for RVMD's oncology pipeline, where Roche provides collaborative development support and Royalty Pharma supplies non-dilutive financing via royalties and debt. Roche maintains a multi-year strategic collaboration with RVMD focused on advancing RAS-targeted precision oncology drugs, including development funding and milestones potentially worth up to 2 billion total to RVMD, without equity ownership or direct royalties for Roche. Royalty Pharma committed up to 2 billion to RVMD in June 2025, comprising $1.25 billion in synthetic royalties on future RAS inhibitor sales (e.g., daraxonrasib) and $750 million in secured debt, enabling RVMD to retain full development and commercialization control. No direct tie exists between Roche & Royalty Pharma specific to RVMD; their interactions are indirect through past royalty purchases on Roche-partnered assets.
1 · Reply
GoPatzGo123
GoPatzGo123 Dec. 5 at 3:14 PM
$ONCY $SMX fux me crazy man congratulations for the folks that bought. People becoming rich overnight
1 · Reply
GoPatzGo123
GoPatzGo123 Dec. 5 at 1:44 PM
$ONCY lol yesterday's gains wiped out in pre market lets see if this can close above a buck ro end the week.
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CaseyLe
CaseyLe Dec. 5 at 1:24 PM
$ONCY this reminds me of Ambryx right before they got bought out. However Oncolytics how’s more going for it. 
1 · Reply
GoPatzGo123
GoPatzGo123 Dec. 5 at 12:38 PM
$SMX $ONCY cancer cure play .
0 · Reply
rexwiggins
rexwiggins Dec. 5 at 10:20 AM
$ONCY 🚀
0 · Reply
Ichigodoran
Ichigodoran Dec. 5 at 10:18 AM
$ONCY Look! new phase new bounce? moving average trending support demand zone. imo. #biotech
0 · Reply
FoxM07
FoxM07 Dec. 5 at 8:39 AM
$ONCY RVMD=$80 per share + runaway success in PDAC. Oncy= not.
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FoxM07
FoxM07 Dec. 5 at 8:38 AM
$ONCY please report notables repetitive, delusional and desperate spam. It's not healthy or realistic.
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Notable_Ex
Notable_Ex Dec. 5 at 2:54 AM
$ONCY Because pelareorep upregulates PD-L1 gene expression which enables pelareorep to turn cold tumors hot, pan-RAS inhibitors, including RVMD's daraxonrasib, will require pelareorep to enhance PD-L1 expression on cancer cell surfaces in order for the pan-RAS inhibitor to be effective.This pan-RAS inhibitors are relegated as second line therapies to pelareorep monotherapy and/or pelareorep combination first line therapy.
0 · Reply
Notable_Ex
Notable_Ex Dec. 5 at 2:53 AM
$ONCY ONCY = $15 Billion is on the basis of RVMD as an inferior comparable, that includes RVMD's daraxonrasib, and other pan-RAS inhibitors, which are unable to effectively treat "cold" tumors and only able to treat cancers with PD-L1 expression of 50% or greater, and 60% with daraxonrasib plus Keytruda and chemo in <50% expressers.
0 · Reply