Sunday, October 4, 2026
Nuvation Bio Update
Thursday, August 6, 2026
Nuvation Bio 2nd Quarter Results
Nuvation Bio (NUVB) is addressing unmet medical need in cancer with lead approved drug Ibtrozi, and clinical testing Safusidenib for high grade glioma. The company released second quarter financial results before market open today. The company is gaining traction with new patients for lead drug Ibtrozi. The drug has been FDA approved for ROS1 NSCLC since June of 2025, and revenues are starting to climb. Some key highlights from the second quarter results below.
Saturday, May 23, 2026
NUVB: Nuvation Bio Update #11
All of Nuvation Bio's previous posts, can be found here Nuvation Posts. The company is addressing the unmet need of ROS1 and high grade glioma, with two unique drugs.
From recent investor conferences that the company has participated, we were given some updated pipeline information. Two updates of interest, include the following for second drug candidate safusidenib.
1. The 40 patient Grade 3 oligodendroglioma which is part of the SIGMA study NCT05303519, has objective response rate as the primary endpoint. The goal of achieving a 20% + response rate in this population, would be seen as positive over standard of care chemotherapy for these patients. The study will be conducted as an Open-Label single arm.
Monday, March 2, 2026
NUVB: Nuvation Bio - Update #9
Nuvation Bio held their 4th quarter conference call today to update investors, on the progress of their cancer drug development programs. Just some key points below, as they will be a multi-year investment, with updates along the way.
- 4th quarter revenue of $41 million, a combination of product and license
- Net loss of $36 million, or 0.11 cents per share with 344 million shares outstanding
- The company is well funded with $529 million in cash and equivalents
- Partner Eisai to file for Ibtrozi ROS1 approval in EU by mid-year 2026
- SIGMA safusidenib 40 patient exploratory cohort, grade 3 oligodendroglioma study with readout expected in 2027
- No revenue guidance announced by the company at this time
Monday, January 12, 2026
NUVB: Nuvation Bio - Update #8
Nuvation Bio has updated investors with the good news of a European partnership, to sell newly FDA approved and commercialized drug Ibtrozi in Europe and other countries outside of the US, for patients with Ros1 NSCLC. Like many other US based companies, they utilize partnerships outside the US who already have a footprint of sales professionals actively selling similar products in the field. Under this agreement completed today with Eisai, there is upfront, milestones and a royalty kick back to the owner of the product, in this case Nuvation Bio. The selling partner reaps the revenue abroad. A win / win cost effective scenario. Below are the Royalty agreements that are now in place outside of the US for Nuvation Bio (NUVB).
(Dovbleron) First and second-line approval.
-Milestone payments based on domestic sales exceeding certain amounts
Sunday, December 7, 2025
NUVB: Nuvation Bio - Update #7
Past Nuvation Bio posts can be found in date order, by clicking here Nuvation Bio.
There are different ways to calculate a stock price target. One way is to use a comparison valuation method. This post considers the current market valuation ($2.932 billion) for Nuvation Bio.
For comparison valuation; In June of 2022 Bristol Myer Squibb offered 4.1 billion to buy Turning Point Therapeutics for their lead drug candidate Repotrectinib a TKI inhibitor for the same indication that Nuvation has been FDA approved for ROS1 NSCLC, BMS News.
Monday, May 19, 2025
NUVB: Nuvation Bio
Nuvation Bio, a development-stage oncology company, focuses on the clinical development for the treatment of cancer. The companies lead drug Taletrectinib, an orally available inhibitor is currently being reviewed by the FDA for Advanced ROS1+NSCLC, with a decision date (PDUFA) of June 23rd.
Financial Statistics:
- $461 million cash
- Debt - minimal
- 340 million diluted shares outstanding
- 782 million market cap
Intellectual Property:
- Taletrectinib - Expected to expire from 2033 to 2042
- Safusidenib - Expected to expire from 2035 to 2041
Timeline Catalyst:
- Taletrectinib: FDA approval decision June 23, 2025
- Safusidenib: Begin pivotal phase 3 for diffuse IDH1-mutant glioma, 2025