pills

Pharma DECODED

Previous edition: 16 May 2024
Share article

Get the full version straight to your inbox.
Exclusive access to our best-in-class data & intelligence
Subscribe now

Moleculin begins NIH-funded Phase II glioblastoma treatment trial

The primary goal of the study is to measure progression-free survival.

Moleculin Biotech has announced the initiation of an investigator-initiated Phase II NU 21C06 clinical trial, funded by the National Institutes of Health (NIH), of WP1066 plus radiation therapy for adults with glioblastoma.

The trial is being conducted under Northwestern University's Investigative New Drug application, which references Moleculin's own US Food and Drug Administration (FDA)-cleared IND in April 2022.

Apart from NIH, BrainUp, a non-profit organisation focusing on creating awareness on brain cancer, is providing additional funding.

The open-label, multi-arm study is focusing on newly diagnosed patients with isocitrate dehydrogenase (IDH) wild-type, O6-methylguanine-DNA methyltransferase (MGMT)-unmethylated glioblastoma.

The primary goal of the study is to measure progression-free survival, while secondary outcomes include the analysis of the tumour microenvironment.

WP1066, an immune/transcription modulator, is designed to enhance the immune response to tumours by hindering regulatory T cells’ errant activity and oncogenic transcription factors.

The asset obtained orphan drug designation for the treatment of brain tumours and rare pediatric disease designation for three other paediatric indications.

Moleculin Biotech chairman and CEO Walter Klemp said: “We are continuing to evaluate WP1066 in additional indications including for the treatment of paediatric brain tumours and look forward to its continued development.”

In November last year, Moleculin reported positive initial efficacy data from the Phase II part of a Phase IB/II clinical trial of Annamycin to treat patients with soft tissue sarcoma (STS) lung metastases.

Latest news

KRAS inhibitors: The next frontier beckons

There has been several developments in the KRAS inhibitor space, shaping the KRAS inhibitors of the future.

FDA approves Bristol Myers Squibb's Breyanzi for follicular lymphoma

The approval is based on results from the open-label, global, multi-centre, single-arm Phase II TRANSCEND FL clinical trial.

Takeda's dengue vaccine obtains WHO prequalification

The TAK-003 vaccine targets all four virus serotypes.

FDA rejects label expansion for Dynavax's hepatitis B vaccine

The US agency rejected the expanded use of Dynavax’s vaccine for adults on haemodialysis, citing insufficient efficacy and safety data.

Tracking the opioid lawsuit settlements amidst calls for oversight

The US National Opioid Settlement is distributing more than $54 billion to communities grappling with the opioid crisis.

Vanda Pharmaceuticals reports positive data from motion sickness trial

In the trial, only 10.4% and 18.3% of the subjects reported vomiting on the 170mg and 85mg doses, respectively.

Allucent receives grant for decentralised Covid-19 vaccine trial

The company received the award to conduct a trial assessing correlates of protection following Covid-19 vaccination.

Strengthen your strategies with industry-specific data

Streamline your sector analysis procedures with market-leading intelligence on companies, trends, innovations, and more, all in one platform.

Book a Demo

Newsletters in other sectors

Aerospace, Defence & Security

BAE wins DARPA contract for microelectronics heat removal
16 May 2024

Automotive

2024 future product report: Ford
16 May 2024

Banking & Payments

Sexism in the City Inquiry
16 May 2024

Explore our market-leading Intelligence Centers

Still looking?

Search companies, themes, reports, as well as actionable data & insights spanning 22 global industries

Explorer

Access more premium companies when you subscribe to Explorer