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1.62 million outstanding unchanged. Show your proof or it didn’t happen.
Wish they would STOP DILUTING this damn stock.
1.62 outstanding unchanged. Proof or it didn’t happen.
Dec. 15, 2022 /PRNewswire/ -- Kintara Therapeutics, Inc. (Nasdaq: KTRA) ("Kintara" or the "Company"), a biopharmaceutical company focused on the development of new solid tumor cancer therapies, today announced it has received Orphan Drug Designation (ODD) from the U.S. Food and Drug Administration (FDA) for VAL-083 for the treatment of diffuse intrinsic pontine glioma (DIPG), a rare and highly-aggressive childhood brain cancer.
The FDA's ODD program provides orphan status to drugs defined as those intended for the treatment, diagnosis or prevention of rare diseases that affect fewer than 200,000 people. ODD provides the sponsor of the drug with development incentives, including tax credits for qualified clinical testing, prescription drug user fee exemptions and seven-year marketing exclusivity upon FDA approval.
"This is another important step for us in evaluating VAL-083 as a treatment for brain tumors in addition to our lead indication of glioblastoma," said Robert E. Hoffman, Kintara's President and CEO. "We will continue with our clinical advancement of the drug candidate with our objective of delivering a much-needed new treatment that can benefit patients."
Volume has dropped BIG time. Screenshot: 
Their priority IS NOT the PPS. It is to SELL THE COMPANY.
Insider Own 1.20% of a Shares Outstanding 1.62M. What does that tell you?
IF management lets this stock sit with NO news for very long traders will think that they are having a HARD TIME getting financing for the final trials phase. That is what I am starting to think. The MM's are having
somewhat a difficult time keeping this in a loop but that will not last very long. Currently they are watching how low the PPS goes because if they let it go too low and news breaks they are in major money trouble.
This week the PPS will drift lower and lower. Think I sell out by Wednesday, Thursday at the latest is no news.
Yes, we will get there regardless. I am extremely bullish on this.
FINVIZ says Target Price $150.00
Undeniably one of the lowest market cap biotech out there that has 80% efficacy for breast cancer. Say hello to 50-60 million dollar market cap fairly soon for starters, by end of next year we will be sitting pretty at triple dollars.
One news will send this instantly above $20.
I think most traders are expecting funding for the last trial.
Hugely bullish on this one. The pattern is similar to SAV*A, not saying it would peak around where SAV*A was a year or two years ago, but something tells me they want to push this 25-30 area and let it sit that range until further data comes out, or better yet, a partnership for funding.
Fantastic close.
Moving like gangbusters now. This float is almost ALL GONE. Currently $13.18.
Up 200%!from the low and my $0.22 shares are almost green again lol.
FINVIZ Target Price 150.00
Totally agree with your estimates.
Anything is possible with that float and especially if the longs truly hold. Someone did some nice numbers on this, they believe this company at current status is worth 30-40 dollars, mid term 100-120 dollars and longer term 900-1200 dollars assuming the share structure stays the same, but we know that won't be the case, but at constant rate we should be in triple digit numbers.
When they publish news about acquiring financing for the trials this PPS will be in the 100's with a float
of ONLY 1.49M.
We should be in the teens by Christmas, next year this goes bonkers. The telling of the story is, no prospectus, shelf offering and no offering, it boils down to what is in the thought process of the insiders, do they know they are worth more than 14 million market? Of course they do, we are destined to hit at bare minimum 50 million market cap for starters and it is going to happened, very confident.
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https://www.kintara.com/
Kintara Therapeutics is focused on developing unique anti-cancer compounds, supported by a strong scientific rationale for development in indications with established biomarkers, and where patients are failing, or are unable to tolerate, current therapies.
VAL-083 is a "first-in-class" small molecule chemotherapeutic. Its unique structure provides many valuable benefits, including the targeting of DNA for its therapeutic effect and its ability to cross the blood brain barrier, critical for activity against central nervous system (CNS) tumors.
VAL-083 has completed Pre-Clinical, Phase I and II trials for the treatment of bevacizumab-refractory glioblastoma multiforme (GBM) and is currently being studied in two Phase II biomarker-driven clinical trials for unmethylated-MGMT GBM.
We are also pursuing the development of VAL-083 in the treatment of ovarian cancer.
REM-001 has broad utility for the treatment of serious cutaneous oncology indications. REM-001 has been previously studied in four Phase 2 and/or Phase 3 clinical trials in patients with cutaneous metastatic breast cancer (“CMBC”), who had previously received chemotherapy and/or failed radiation therapy.
Zacks Small-Cap Research
https://s27.q4cdn.com/906368049/files/News/2021/Zacks_SCR_Research_10112021_KTRA_Vandermosten.pdf
Based on our DCF model and a 15% discount rate, Kintara Therapeutics is valued at approximately $5.25 per share. Our model applies a 60% probability for VAL-083 in unmethylated GBM, a 50% probability in methylated GBM and a 50% probability of approval and commercialization in REM-001 for CMBC. The model includes contributions from the United States and Europe. Other regions will be included upon further clarity.
Shares Outstanding (mil) 43.2
Current Price (10/8/2021) $0.77
Valuation $5.25.
11/03/21
Thanks to its promising pipeline and $0.88 share price, 5-star analyst Michael King, of
H.C. Wainwright, sees an attractive entry point for investors.
“We are bullish about KTRA shares for the following five reasons
: (1) The GBM AGILE trial tests VAL-083 in
all three subtypes of GBM, allowing for multiple opportunities for VAL-083 to prove its
efficacy against phenotypically distinct types of the disease.
(2) VAL-083 is a bifunctional
alkylating agent that crosses the blood brain barrier and exhibits very favorable pharmacologic
properties relative TMZ; fulfilling the need for systemic availability in the brain.
(3) VAL-083
has an established favorable safety record, both from initial trials and prior clinical use in
multiple indications.
(4) Dire unmet need in GBM may present relatively low bar for approval.
(5) Phase 3 ready REM-001 is an additional bonus which is not factored into our valuation
assumptions and could potentially deliver value to shareholders while providing a backstop
against downside,” King explained.
