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Scancell taps Nasdaq reverse merger to fund Phase III melanoma program

UK-based Scancell Holdings plc (AIM: SCLP) has announced an all-share merger agreement with Burlington, Massachusetts-based Neuphoria Therapeutics Inc....

Scancell taps Nasdaq reverse merger to fund Phase III melanoma program

UK-based Scancell Holdings plc (AIM: SCLP) has agreed to acquire Burlington, Massachusetts-based Neuphoria Therapeutics Inc. (Nasdaq: NEUP) in an all-share merger that will give the combined company a Nasdaq listing under the ticker SCLT while retaining Scancell's existing AIM listing. Neuphoria is primarily contributing its Nasdaq listing, closing cash and legacy partnered assets following the failure of its lead neuropsychiatric program. The transaction is backed by financing of up to USD 89 million to support the registrational Phase III development of Scancell's melanoma immunotherapy iSCIB1+.

The all-share merger sees Neuphoria becoming an indirect wholly owned subsidiary of Scancell upon completion. Neuphoria stockholders will also receive contingent value rights covering potential proceeds from legacy partnered assets, including agreements with Merck and a Pfizer-linked KAT6 program, as well as certain IP monetization and an Australian R&D tax credit.

Alongside the merger, Scancell expects to secure up to USD 89 million through a combination of equity financing, debt facilities and Neuphoria's closing cash. The package includes a USD 39.1 million private placement, a USD 12.0 million UK placing, a non-binding term sheet with funds managed by BlackRock for up to USD 25.0 million in debt financing, and a minimum of USD 10.0 million in cash expected to be contributed by Neuphoria at closing.

iSCIB1+ is a plasmid DNA ImmunoBody that encodes tumour-associated antigens to drive tumour-specific T-cell immunity, administered needle-free intramuscularly. In the Phase II SCOPE study (NCT04079166), iSCIB1+ in combination with nivolumab and ipilimumab demonstrated 77% progression-free survival at 22 months in patients with unresectable Stage IIIB/IV melanoma selected by HLA allele. The FDA cleared the IND application for the global Phase III trial in January 2026 and granted Fast Track Designation; the Phase III trial is expected to initiate in H2 2026.

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The merger also follows a series of setbacks at Neuphoria. In October 2025, the company's lead candidate BNC210 failed the Phase III AFFIRM-1 trial in social anxiety disorder. More recently, Merck discontinued the Phase II Alzheimer's disease trial of partnered α7 nicotinic acetylcholine receptor modulator MK-1167 after a planned interim analysis found insufficient efficacy to support further development, although Merck said the broader collaboration remains in place.

For Scancell, the merger provides a faster route to the US public markets and access to specialist oncology investors ahead of its planned registrational melanoma trial. The firm is the latest in a growing group of clinical-stage biotechs using reverse mergers with Nasdaq-listed peers to access US investors while funding late-stage clinical development. Examples include Avenzo Therapeutics' reverse merger with Rallybio alongside a USD 215 million private placement in June 2026, and Remix Therapeutics' merger with Passage Bio with a concurrent USD 100 million raise. For Scancell, the Nasdaq listing is explicitly framed as access to US oncology investors ahead of a registrational trial in a competitive melanoma landscape where checkpoint inhibitor combinations remain the standard of care.


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