81vette
9月前
NCNA,bio pharma,zero borrow,post r s play,2m float,moving freely,10Xs relative volume is key here,institutional buying up 80%,excellent chart,bottom reversal,went up in death hr,watch for volume surges any minute ,had pops to $5 pre-mkt
I am in 4.05
Good skill everyone!!
JusDePomme
11月前
NuCana Reports First Quarter 2025 Financial Results and Provides Business Update
Initiation of Expansion Study of NUC-7738 in Combination with Pembrolizumab for Patients with PD-1 Inhibitor-Resistant Melanoma
Initial Data from the Expansion Study of NUC-7738 Expected in Q4 2025 with Final Data in 2026
Additional Data from the Ongoing Phase 1b/2 Study of NUC-3373 in Combination with Pembrolizumab Remain on track for 2025
Anticipated Cash Runway Extended into Q4 2026 to Support Key Value-Driving Milestones and Complete the Expansion Study of NUC-7738
EDINBURGH, United Kingdom, June 02, 2025 (GLOBE NEWSWIRE) -- NuCana plc (NASDAQ: NCNA) announced financial results for the first quarter ended March 31, 2025 and provided an update on its clinical development program with its two lead anti-cancer medicines.
“We have entered 2025 with a clear focus on the advancement of our pipeline through key milestones, into late-stage development, and towards commercialization,” said Hugh S. Griffith, NuCana’s Founder and Chief Executive Officer. “Our lead program, NUC-7738, continues to show significant promise. NUC-7738 is a novel agent that profoundly impacts gene expression in cancer cells and targets multiple aspects of the tumor microenvironment. In our ongoing Phase 1/2 NuTide:701 study, we have observed a favorable safety profile, meaningful tumor volume reduction and prolonged progression free-survival in patients with PD-1 inhibitor refractory and resistant metastatic melanoma. Based on these compelling results, we have recently initiated an expansion trial of NUC-7738 in an additional 28 patients with PD-1 inhibitor-resistant melanoma, that supports our registrational path. Based on this, we plan to meet with the U.S. Food and Drug Administration to determine the optimal regulatory strategy forward towards commercialization.”
Mr. Griffith continued, “Turning to our second program, NUC-3373 is a targeted thymidylate synthase inhibitor with immune modulating properties. We are encouraged by the data from the ongoing Phase 1b/2 NuTide:303 study. This study is evaluating NUC-3373 in combination with pembrolizumab in patients with advanced solid tumors, and NUC-3373 with docetaxel in patients with lung cancer. To date, we have seen notable tumor volume reductions and prolonged progression free survival in these patients. We look forward to sharing additional data from this trial later this year.”
Mr. Griffith concluded, “Lastly, we strengthened our balance sheet with a financing in May, extending our cash runway through key value-driving milestones. With multiple data readouts ahead, we are well-positioned to deliver on our mission of improving treatment outcomes for patients with cancer.”
2025 Anticipated Milestones
NUC-7738 Initiate an expansion of the Phase 1/2 study (NuTide:701) of NUC-7738 in combination with pembrolizumab in patients with PD-1 inhibitor-resistant melanoma;Announce data from the Phase 1/2 expansion study (NuTide:701) of NUC-7738 in combination with pembrolizumab; andObtain regulatory guidance from the U.S. Food and Drug Administration on pivotal study design for NUC-7738 in melanoma.
NUC-3373 Announce additional data from the Phase 1b/2 modular study (NuTide:303) of NUC-3373 in combination with pembrolizumab in patients with solid tumors.
First Quarter 2025 Financial Highlights and Cash Position
As of March 31, 2025, NuCana had cash and cash equivalents of £4.0 million compared to £6.7 million at December 31, 2024. Subsequent to March 31, 2025, NuCana
Renee
11月前
NCNA: from the June 27th Prospectus: Ordinary shares to be outstanding immediately after this offering
34,540,891,147 ordinary shares (including those ordinary shares represented by ADSs), assuming no Series A ADS Purchase Warrants, or Series A Warrants, are exercised.
That's a lot o' shares!!!
https://www.sec.gov/edgar/search/#/ciks=0001709626&entityName=NuCana%2520plc%2520(NCNA)%2520(CIK%25200001709626)
Gatorhide
1年前
Someone on here said Merck was going to present a deal in two weeks. Instead of calling bullshit, I did my research. Meanwhile, the FDA gives Merck “flagship approval” to use its top-selling drug Keytruda. So what, right? Well, let a monkey be my uncle—it just so happens Merck’s FDA approval to expand Keytruda’s use in resectable head and neck squamous cell carcinoma (PD-L1?≥1)—its first perioperative label in this cancer type—is a tailwind for NuCana’s Keytruda-based collaborations. Broader Keytruda use raises baseline demand. As oncologists adopt it in new settings, combo trials like NUC-3373 and NUC-7738 gain traction among prescribers and trial designers. Stronger biotech partnership perception. An expanding label reflects Merck’s confidence in Keytruda’s combinability—NuCana benefits by association, boosting investor and CRO interest. NuCana’s ProTide candidates are built to complement PD-1 blockade. More approved uses ease integration into regimens.